MEDICATED- menthol and zinc oxide powder 
Target Corporation

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 Ingredients

Active ingredients

Menthol 0.15%

Zinc oxide 1.0%

Purpose

Purpose

External analgesic

Skin protectant

Uses

Uses for the temporary relief of paina and itching due to:

dries the oozing and weeping of:

Warnings

Warnings

For external use only

When using

When using this product avoid contact with the eyes

Stop use

Stop use and ask a doctor if conditin 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

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 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

Inactive ingredients

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

Questions

Questions? Call 1-800-910-6874

disclaimer

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

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

Made in the USA with US and foreign components

Adverse Reactions

Distributed by Target Corporation

Minneapolis, MN 55403

Shop Target.com

Principal display panel

NDC 11673-551-38

body powder

medicated

compare to Gold bond

Medicated Body Powder

helps with temporary relief of pain and itchng

external analgesic/skin protectant

pleasantly scented with an essential oil blend

up + up

NET WT 10 OZ (283.5 g)

image description

MEDICATED 
menthol, zinc oxide powder
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-551
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.5 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 10 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-551-38 283.5 g in 1 BOTTLE, DISPENSING
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 07/30/2003
Labeler - Target Corporation (006961700)
Registrant - Vi-Jon (790752542)
Establishment
Name Address ID/FEI Business Operations
M+K Packaging 047022405 manufacture(11673-551)

Revised: 1/2013
Document Id: 73149505-a2aa-4f13-bdce-65a4299b5303
Set id: aa6a0d0c-9402-4bb2-b40e-73d1a937f2ae
Version: 1
Effective Time: 20130121
 
Target Corporation