BODY- menthol, zinc oxide powder 
Walgreen Co.

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.

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Drug Facts

Active ingredient

Active ingredients

Menthol 0.15%

Zinc oxide 1.0%

Purpose

Purpose

External analgesic

Skin protectant

Uses

Uses for temporary relief of pan and itching due to:

dries the oozing and weeping of:

warnings

Warnings

For external use only

When using this product

When using this product avoid contact with the eyes

Stop use and ask a doctor

Stop use and ask a doctor if condition worsens, or if symtpoms persist for more than 7 days or clear up and occur again within a few days

keep out of reach of children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

adults and children 2 year of age and older - apply to affected area not more than 3 to 4 times daily

children under 2 years of age - do not use, consult a doctor

Inactive ingredients

Inactive ingredients talc, acacia, eucaluptol, methyl salicylate, salicylic acid, thymol, zinc stearate

Questions

Questions? Call 1-888-593-0593

Disclaimer

Ths product is not manufacgtured or distributed by Chattem, Inc., owener of the registered tradmark of Gold Bond

This produc is sold by weight, not by volume.  Some settling may occur during handling and shipping

Adverse reactins

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD, DEERFIELD, IL 60015

100% SATISFACTIN GUARANTEED

walgreens.com

MADE IN U.S.A. WITH U.S. AND FOREIGN COMPONENTS

Principal Display Panel

Studio 35

MEDICATED

BODY POWDER

SKIN PROTECTANT

EXTERNAL ANALGESIC

COOLING, ABSORBING

+ ITCH RELIEVING

Compare to Gold Bond Medicated Body Powder active ingredient

NET T 10 OZ (283 g)

image description

BODY 
menthol, zinc oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0551
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.5 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
ACACIA (UNII: 5C5403N26O)  
EUCALYPTOL (UNII: RV6J6604TK)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
THYMOL (UNII: 3J50XA376E)  
ZINC STEARATE (UNII: H92E6QA4FV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0551-38283 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/31/2003
Labeler - Walgreen Co. (008965063)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIBusiness Operations
MK Packaging047022405manufacture(0363-0551)

Revised: 3/2013
Document Id: 1c9084b2-84b3-436b-ab20-b893129c245d
Set id: 595fb3a3-36f8-48f8-9dfd-e1f70376b66c
Version: 1
Effective Time: 20130318
 
Walgreen Co.