DRUG FACTS

DR. WALTONS BABY POWDER- talc powder
Dr. Waltons, Incorporated

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

DRUG FACTS

KEEP OUT OF CHILDREN'S REACH. AVOID BABY'S EYES, NOSE AND MOUTH.

GREAT FOR YOUR BABY: PREVENTS AND SOOTHES DIAPER RASH, ELIMINATES ODOR. USE AFTER EVERY BATH AND DIAPER CHANGE.

GREAT FOR YOU: USE DAILY FOR SOFT, IRRITATION-FREE SKIN. REDUCES CHAFING AND ABSORBS MOISTURE. GREAT FOR ELIMINATING SAND AND MOISTURE AFTER A DAY AT THE BEACH!

CAUTION: KEEP OUT OF CHILDREN'S REACH. AVOID BABY'S EYES, NOSE AND MOUTH. NOT FOR USE ON BROKEN SKIN. IF IRRITATION DEVELOPS, PLEASE DISCONTINUE USE.

HYPOALLERGENIC; DERMATOLOGIST AND ALLERGY TESTED; PEDIATRICIAN TESTED

IF IRRITATION DEVELOPS, PLEASE DISCONTINUE USE.

PREVENTS AND SOOTHES DIAPER RASH, ELIMINATES ODOR

SHAKE POWDER ONTO HANDS AND GENTLY RUB ONTO SKIN

TALC

VITAMIN E (ALPHA-TOCOPHEROL), ZINC OXIDE

image of front label image of back label Enter section text here

DR. WALTONS BABY POWDER
talc powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76271-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (ALPHA-TOCOPHEROL - UNII:H4N855PNZ1)	ALPHA-TOCOPHEROL	5.2 g in 675 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5.13 g in 675 g

Ingredient Name	Strength
Inactive Ingredients
TALC (UNII: 7SEV7J4R1U)

#	Item Code	Package Description
Packaging
1	NDC:76271-001-24	675 g in 1 BOTTLE, PLASTIC
2	NDC:76271-001-02	55 g in 1 BOTTLE, PLASTIC

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part347	07/09/2011

Labeler - Dr. Waltons, Incorporated (041377104)