NDC | 49035-840-01 |
Set ID | 907d44c5-cbd1-4d13-8c5c-c164f7a536e5 |
Category | HUMAN OTC DRUG LABEL |
Packager | Wal-Mart |
Generic Name | |
Product Class | Aminoglycoside Antibacterial |
Product Number | |
Application Number | PART333B |
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Use
-
Warnings
For external use only.
Not for prolonged use.
Do not use
- in the eyes, nose, or over large areas of the body
- if you are allergic to any of the ingredients
- longer than 1 week unless directed by a doctor
-
Directions
Adults and children 2 years of age and older:
- clean the affected area
- apply a 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
- the affected area may be covered with a sterile bandage
Children under 2 years of age: consult a doctor
- Other information
- Inactive ingredient
- Questions or comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
NDC 49035-840-01
equate™
Compare
Neosporin®
+ Pain Relief
Active
Ingredients*Maximum Strength
First Aid
Antibiotic
+ Pain ReliefFirst Aid Antibiotic
Pain Relieving
OintmentBacitracin Zinc, Neomycin
Sulfate, Polymyxin B Sulfate,
Pramoxine HCl- Soothes painful cuts,
scrapes and burns while
preventing infection
NET WT 1 OZ (28g)
- Soothes painful cuts,
-
INGREDIENTS AND APPEARANCE
EQUATE FIRST AID ANTIBIOTIC PLUS PAIN RELIEF
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-840 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Bacitracin Zinc (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [USP'U] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-840-01 1 in 1 CARTON 10/18/2018 1 28 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 10/18/2018 Labeler - Wal-Mart (051957769) Establishment Name Address ID/FEI Business Operations Natureplex LLC 062808196 MANUFACTURE(49035-840)