NDC | 72663-140-32 |
Set ID | d4186754-ed6a-4c59-b841-8f4d7b880cd1 |
Category | HUMAN OTC DRUG LABEL |
Packager | Welly Health PBC |
Generic Name | |
Product Class | Amide Local Anesthetic, Aminoglycoside Antibacterial, Antiarrhythmic |
Product Number | |
Application Number | PART333E |
- Instant Hand Sanitizer Gel
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
- Triple Antibiotic Ointment
- Active Ingredient (in each gram)
- Purpose
- Uses
-
Warnings
For external use only
Do not use:
- internally
- in eyes
- over large areas of the body or on puncture wounds, animal bites or serious burns
- for more than 1 week unless directed by a doctor
- if you are allergic to any of the ingredients
Stop use and ask a doctor if
- a rash or allergic reactions develops
- condition worsens or persists
- Directions
- Inactive Ingredients
- Burn Gel
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- 1% Hydrocortisone Cream
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
-
SPL UNCLASSIFIED SECTION
ASSORTED FIRST AID OINTMENTS
ASSORTED SINGLE USE PACKETS
Distributed by: Welly Health PBC
Minneapolis, MN 55402
1-833-BE-WELLYRecycle me!
WellyTM www.GetWelly.com
Superhero Supplies
9 - HAND SANITIZER 0.9g (1/32 OZ)
9 - TRIPLE ANTIBIOTIC 0.5g (1/57 OZ)
9 - BURN GEL 0.9G (1/32 OZ)
9 - 1% HYDROCORTISONE 0.9g (1/32 OZ)
- Packaging
-
INGREDIENTS AND APPEARANCE
WELLY SUPERHERO SUPPLIES KIT
alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine hydrochloride, hydrocortisone kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72663-140 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72663-140-32 1 in 1 KIT; Type 0: Not a Combination Product 03/01/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 9 POUCH 8.1 mL Part 2 9 POUCH 4.5 mL Part 3 9 POUCH 8.1 mL Part 4 9 POUCH 8.1 mL Part 1 of 4 ANTISEPTIC
alcohol gelProduct Information Item Code (Source) NDC:72663-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 666 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 mL in 1 POUCH; 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 part333E 02/25/2019 Part 2 of 4 ANTIBIOTIC
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointmentProduct Information Item Code (Source) NDC:72663-560 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 6.0 mg in 1 mL NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 mL POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 0.77 mg in 1 mL Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.5 mL in 1 POUCH; 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 02/25/2019 Part 3 of 4 ANALGESIC
lidocaine hydrochloride gelProduct Information Item Code (Source) NDC:72663-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 2 g in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 mL in 1 POUCH; 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 02/25/2019 Part 4 of 4 ANTI-ITCH
hydrocortisone creamProduct Information Item Code (Source) NDC:72663-580 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 g in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PARAFFIN (UNII: I9O0E3H2ZE) PETROLATUM (UNII: 4T6H12BN9U) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) WHITE WAX (UNII: 7G1J5DA97F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 0.9 mL in 1 POUCH; 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 02/25/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/01/2019 Labeler - Welly Health PBC (116766884)