NDC | 72663-130-23 |
Set ID | 55f717e6-764e-444c-aa70-517174b7553f |
Category | HUMAN OTC DRUG LABEL |
Packager | Welly Health PBC |
Generic Name | |
Product Class | Aminoglycoside Antibacterial |
Product Number | |
Application Number |
- 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 other allergic reaction develops
- condition worsens or persists
- Directions
- Inactive Ingredients
- 1% Hydrocortisone Cream
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Instant Hand Sanitizer Gel
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
-
SPL UNCLASSIFIED SECTION
FIRST AID TRAVEL KIT
ASSORTED BANDAGES & OINTMENTS
First aid kit sized for travel with everything you'll need and nothing you won't.
- Flexible fabric bandages in two sizes and a few colors to cover cuts and scratches.
- Hand Sanitizer helps keep hands clean when there's no sink in sight.
- Triple Antibiotic ointment helps prevent infection.
- 1% Hydrocortisone anti-itch ointment helps relieve skin irritation and rashes.
Product not made with natural rubber latex.
Bandages are sterile unless individual wrapper opened or damaged.Distributed by: Welly Health PBC
Minneapolis, MN 55402
1-833-BE-WELLYRecycle me!
WellyTM www.GetWelly.com
Human Repair Kit
15 BANDAGES - 3/4 x 3 IN (1.9 x 7.6 CM)
15 BANDAGES - 5/8 X 2 1/4 IN (1.6 X 5.7 CM)
3 - TRIPLE ANTIBIOTIC 0.5g (1/57 OZ)
3 - 1% HYDROCORTISONE 0.9g (1/32 OZ)
6 - HAND SANITIZER 0.9g (1/32 OZ)
- Packaging
-
INGREDIENTS AND APPEARANCE
WELLY HUMAN REPAIR KIT
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, hydrocortisone, alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72663-130 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72663-130-23 1 in 1 KIT; Type 1: Convenience Kit of Co-Package 03/01/2019 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 3 POUCH 1.5 mL Part 2 3 POUCH 2.7 mL Part 3 6 POUCH 5.4 mL Part 1 of 3 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 2 of 3 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 Part 3 of 3 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 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2019 Labeler - Welly Health PBC (116766884)