STUDIO 35 MEDICATED BODY- menthol 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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Walgreens 379.001 379AB

Active ingredients

Menthol 0.15%

purpose

External analgesic

Uses

for the temporary relief of pain and itching due to:

  • minor cuts
  • poison ivy
  • scrapes
  • sunburn
  • poison oak
  • minor burns
  • insectd bites
  • poison sumac
  • minor skin irritations

Warnings

For external use only

When using this product

avoid contact with the eyes

stop use and ask a doctor

if condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center Right Away

Directions

adults and children 2 years 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

  • for best results dry area thoroughly before applying

inactive ingredients

talc, zinc oxide, acacia seyal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate

Questions?

Call 1-800-925-4733

Disclaimer

This product is not manufactured or distributed by Chattem, distributor of Gold Bond Medicated Body Powder.

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

Adverse Reactions Section

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RE., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

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

379.000/379AA

principal display panel

COMPARE TO

GOLD BOND MEDICATED BODY POWDER

Studio 35

MEDICATED

BODY POWDER

EXTERNAL ANALGESIC

COOLING

ITCH RELEIF

ABSORBS MOISTURE

PLEASANTLY SCENTED WITH AN ESENTIAL OIL BLEND

NET WT 10 OZ (283 g)

image description

STUDIO 35 MEDICATED BODY 
menthol powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0043
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
GUM TALHA (UNII: H18F76G097)  
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:0363-0043-38283 g in 1 BOTTLE; Type 0: Not a Combination Product03/04/201404/30/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/04/201404/30/2021
Labeler - Walgreen Co (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
MK Packaging047022405manufacture(0363-0043)

Revised: 4/2021
 
Walgreen Co