NDC | 44224-0001-2, 52124-0001-1, 52124-0003-1, 52124-0013-1, 52124-0014-1, 52124-0040-1, 69842-200-00 |
Set ID | 44bc7046-4a72-7085-e054-00144ff8d46c |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS |
Generic Name | |
Product Class | Amide Local Anesthetic, Aminoglycoside Antibacterial, Antiarrhythmic |
Product Number | |
Application Number | PART333A |
- Active Ingredients - Genuine Triple Antibiotic
- Purpose - Genuine Triple Antibiotic
- Uses - Genuine Triple Antibiotic
- Warnings - Genuine Triple Antibiotic
- DO NOT USE - Genuine Triple Antibiotic
- Stop Use - Genuine Triple Antibiotic
- Keep Out of Reach of Children - Genuine Triple Antibiotic
- Directions - Genuine Triple Antibiotic
- Storage and Handling - Genuine Triple Antibiotic
- Inactive Ingredients - Genuine Triple Antibiotic
- Active Ingredients - Antiseptic
- Purpose - Antiseptic
- Use - Antiseptic
- Warnings - Antiseptic
- Keep out of reach of children - Antiseptic
- Stop Use - Antiseptic
- Do Not Use - Antiseptic
- Directions - Antiseptic
- Inactive Ingredients - Antiseptic
- Active Ingredient - Ibuprofen
- Purpose - Ibuprofen
- Uses - Ibuprofen
-
Warnings - Ibuprofen
Allergy alert : Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: shock, facial swelling, asthma (wheezing) rash, skin reddening, blisters, hives If an allergic reaction occurs, stop use and seek medical help right away.
Stomach bleeding warning: This product contains a nonsteroidal anti-inflammatory drug (NSAID), which may cause severe stomach bleeding. The chance is higher if you: are age 60 or older, have had stomach ulcers or bleeding problems, take a blood thinner (anticoagulant) or steroid drug, take other drugs containing NSAIDs (aspirin, ibuprofen, naproxen, or others), have 3 or more alcoholic drinks every day while using this product, take more or for a longer time than directed - Do Not Use - Ibuprofen
-
Ask a Doctor - Ibuprofen
Ask a doctor before use if stomach bleeding warning applies to you; you have a history of stomach problems such as heartburn; you have a high blood pressure, heart disease, liver cirrhosis, or kidney disease; you are taking a diuretic
Ask a doctore before use if you are taking any other drug containing NSAID (prescription or nonprescription); taking aspirin for heart attack or stroke, because Ibuprofen may decrease this benefit of aspirin; taking any other drug
- When Using - Ibuprofen
-
Stop Use - Ibuprofen
Stop use and ask a doctor if you experience any of the following signs of stomach bleeding; feel faint; vomit blood; have bloody or black stools; have stomach pain that does get better; pain gets worse or lasts more than 10 days; fever gets worse or lasts more than 3 days; redness or swelling is present in the painful area; any new symptoms appear
- Pregnancy or Breast Feeding - Ibuprofen
- Keep out of reach of Children - Ibuprofen
-
Directions - Ibuprofen
do not use more than directed; the smallest effective dose should be used; do not take longer than 10 days, unless directed by a doctor.
Adults and Children (12 years and older): Take 1 tablet every 4 to 6 hours while symptoms persist. If pain or fever does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets in 24 hours, unless directed by a doctor.
Children under 12 years: Do not give to children under 12 years of age. - Other Information
- INACTIVE INGREDIENTS - Ibuprofen
- Active Ingredients - Non-Aspirin
- Purpose - Non Aspirin
- Uses - Non Aspirin
-
Warnings - Non Aspirin
Liver warning: This product contains acetaminophen.
Severe liver damage may occur if: adult takes more than 12 tablets in 24 hours, which is the maximum daily amount; child takes more than 5 doses in 24 hours; taken with other drugs containing acetaminophen; adult has 3 or more alcoholic drinks every day while using this product
- Do Not Use - Non Aspirin
- Ask a Doctor - Non Aspirin
- Stop Use - Non Aspirin
- Pregnancy - Non Aspirin
- Keep Out of Reach of Children - Non Aspirin
- Inactive Ingredients - Non Aspirin
-
Directions - Non Aspirin
Directions
Adults and Children Take 2 tablets every 4 to 6 hours as
12 years of age needed. Do not take more than 12 tablets
or older in 24 hours.
Children 6-11 years Take 1 tablet every 4 to 6 hours as
of age needed. Do not take more than 5
tablets in 24 hours.
Children under 6 Do not use this regular strength product.
years of age This will provide more than the
recommended dose (overdose) and could
cause serious health problems.
- Storage and Handling - Non Aspirin
- Active Ingredients - Burn Cream
- Purpose - Burn Cream
- Uses - Burn Cream
- Warnings - Burn Cream
-
Do Not Use - Burn Cream
Do not use: In eyes, in large quantities, over raw blistered areas, or on deep puncture wounds, animal bites or serious burns, for more than one week
Do not use:
in the eyes or apply over large areas of the body.
longer than 1 week unless directed by a doctor.
in large quantities, particularly over raw surfaces or blistered areas.
Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.
When using this product, avoid contact with the eyes. - Stop Use - Burn Cream
- Keep Out of Reach of Children
- Directions - Burn Cream
- Storage and Handling - Burn Cream
- Inactive Ingredients - Burn Cream
- Active Ingredients - After Bite
- Purpose - After Bite
- Uses - After Bite
- Warnings - After Bite
- Keep Out of Reach of Children - After Bite
- Stop Use - After Bite
- When Using - After Bite
- DIrections - After Bite
- First Aid Kit Sleeve
- Principal Display Panel - Triple Antibiotic
- Package Label - Antiseptic
- Package Label - Ibuprofen
- Package Label Non Aspirin
-
Package Label - Burn Cream
Genuine First Aid Burn Cream
Antiseptic Pain Relief With Aloe
Net Wt 0.9g (1/32 oz)
Manufactured in CHINA for
Genuine First AidGFA Production Xiamen Co., Ltd
No. 20 Huli Industrial Park, Meixi Road, Tong'an, Xiamen, Fujian, China 361100
Tel: 86-592-7269515 Fax: 86-592-7269528 Http: //www.gfaproduction.com - Package Label - After Bite
-
INGREDIENTS AND APPEARANCE
CVS FIRST AID KIT
diphenhydramine hydrochloride, aspirin, isopropyl alcohol, bacitracin zinc, neomycin sulfate, polymyxin b, benzalkonium chloride, ammonia, lidocaine, acetaminophen, ibuprofen, kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-200 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-200-00 1 in 1 BAG; Type 0: Not a Combination Product 12/28/2016 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 4 PACKAGE 3 mL in .7 Part 2 2 PACKET 2 g in .9 Part 3 1 PACKAGE 2 Part 4 1 PACKET 2 Part 5 15 PACKAGE 12 mL in .8 Part 6 6 TUBE 3 g in .5 Part 1 of 6 AFTER BITE WIPE
ammonia swabProduct Information Item Code (Source) NDC:44224-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE 1000 (UNII: MCU2324216) LIGHT MINERAL OIL (UNII: N6K5787QVP) C12-13 ALCOHOLS (UNII: T7ZJT3I9X2) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-0001-2 0.7 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/28/2016 Part 2 of 6 GENUINE FIRST AID BURN ANTISEPTIC PAIN RELIEF WITH ALOE
benzalkonium chloride, lidocaine creamProduct Information Item Code (Source) NDC:52124-0040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0040-1 0.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/28/2016 Part 3 of 6 NON-ASPIRIN
acetaminophen tabletProduct Information Item Code (Source) NDC:52124-0014 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STARCH, CORN (UNII: O8232NY3SJ) POVIDONE (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape ROUND Size 11mm Flavor Imprint Code AZ;234 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0014-1 2 in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 12/28/2016 Part 4 of 6 IBUPROFEN
ibuprofen tabletProduct Information Item Code (Source) NDC:52124-0013 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) STEARIC ACID (UNII: 4ELV7Z65AP) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYDEXTROSE (UNII: VH2XOU12IE) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRIACETIN (UNII: XHX3C3X673) POWDERED CELLULOSE (UNII: SMD1X3XO9M) HYPROMELLOSES (UNII: 3NXW29V3WO) LACTOSE (UNII: J2B2A4N98G) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color white Score no score Shape ROUND Size 10mm Flavor Imprint Code 44;352 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0013-1 2 in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075010 12/28/2016 Part 5 of 6 ANTISEPTIC
benzalkonium chloride swabProduct Information Item Code (Source) NDC:52124-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0001-1 0.8 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/28/2016 Part 6 of 6 GENUINE TRIPLE ANTIBIOTIC
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointmentProduct Information Item Code (Source) NDC:52124-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) WATER (UNII: 059QF0KO0R) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0003-1 0.5 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 12/28/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/28/2016 Labeler - CVS (062312574) Establishment Name Address ID/FEI Business Operations Tender Corporation 064437304 manufacture(69842-200)