NDC | 44224-0203-1, 52124-0001-1, 52124-0003-1, 52124-0008-1, 52124-0017-1 |
Set ID | 4ad9d0a5-cd17-0808-e054-00144ff8d46c |
Category | HUMAN OTC DRUG LABEL |
Packager | Tender Corporation |
Generic Name | |
Product Class | Aminoglycoside Antibacterial |
Product Number | |
Application Number | PART333A |
- Active Ingredient - Antiseptic
- Purpose - Antiseptic
- Use - Antiseptic
-
Warnings, Precautions and Directions - Antiseptic
For External use only.
Keep out of Reach of Children.
Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.
Do not uses in eyes or over large areas of the body.
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
- Inactive Ingredients - Antiseptic
- Active Ingredient - Alcohol Prep Pad
- Use - Alcohol Prep Pad
-
Warnings, Precautions and Directions - Alcohol Prep Pad
For External Use Only
Flammable - Keep away from fire or flame
Do Not Use - with electrocautery, in eyes
Stop Use and Ask a Doctor if - Irritation or redness develop and persists for more than 72 hours
Keep out of Reach of Children
If swallowed, get medical help or contact a poison control center right away.
Tear Open packet, unfold and use as and wipe injection site vigorously and discard.
Store at Room Temperature
- Active Ingredients - Insect Relief Pad
- Purpose - Insect Relief Pad
- Use - Insect Relief Pad
-
Warnings, Precautions and Directions - Insect Relief Pad
Clean intended area thoroughly with pad. Discard after single use
Warnings: For external use only.
Avoid contact with eyes. If this happens, rinse thoroughly with water
If swallowed, get medical help or contact a Poison Control Center right away
Flammable - keep away from fire or flame
Do not use: In eyes, on broken skin, deep puncture wounds. If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.
- Active Ingredients - Triple Antibiotic Ointment
- Purpose - Triple Antibiotic Ointment
- Use - Triple Antibiotic Ointment
-
Warnings, Precautions and Directions - Triple Antibiotic Ointment
For external use only.
Do not use: in eyes; over large areas of the body;
If allergic to any of the ingredients; for more than one week unless directed by a physician
Stop use and consult a doctor: if the condition persists or gets worse; a rash or other allergic reaction develops.
Keep out of reach of children.
If ingested, contact a Poison Control Center right away
Directions: clean affected area; apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage.
- Adventure First Aid .5 Tin
-
INGREDIENTS AND APPEARANCE
ADVENTURE FIRST AID .5 TIN
benzocaine, alcohol, benzalkonium chloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-0203 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-0203-1 1 in 1 BOX; Type 0: Not a Combination Product 10/01/2015 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 PACKAGE 1 mL in .5 Part 2 4 PACKAGE 3 mL in .7 Part 3 4 PACKAGE 3 mL in .8 Part 4 4 TUBE 2 g in .5 Part 1 of 4 INSECT STING RELIEF PAD
benzocaine,alcohol swabProduct Information Item Code (Source) NDC:52124-0008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 0.6 mg in 100 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0008-1 0.5 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 04/23/2011 Part 2 of 4 ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Item Code (Source) NDC:52124-0017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 700 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:52124-0017-1 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 part333A 02/01/2016 Part 3 of 4 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 04/23/2010 Part 4 of 4 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 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 BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [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 10/01/2015 Labeler - Tender Corporation (064437304) Registrant - Tender Corporation (064437304) Establishment Name Address ID/FEI Business Operations Tender Corporation 064437304 manufacture(44224-0203)