MEDICATED BODY POWDER- menthol powder 
Walmart Stores Inc

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Equated Medicated Body Powder - 202

Drug Facts

Active Ingredients

Menthol 0.15 %

Purpose

External Analgesic

Uses

for the temporary relief of the pain and itch associated with

  • minor cuts
  • scrapes
  • sunburn
  • insect bites
  • prickly heat
  • rashes
  • minor burns
  • minor skin irritations
  • dries the oozing of poison ivy, oak and sumac.

Warnings

For external use only

When usin this product

Avoid contact with eyes. Not for genital area.

Stop use and ask a doctor if

  • condition worsens
  • Redness, irritation, swelling or pain persist or increases
  • symptoms do not get better within 7 days or clear up and occur again within a few days

Keep out of reach of children

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • adults and children 2 years of age and over, apply freely up to 3 or 4 times daily
  • Children under 2 years: consult a physician
  • for best results, dry skin thoroughly before use

Inactive Ingredients

acacia seyl gum, eucalyptol, methyl salicylate, salicylic acid, sodium bicarbonate, thymol, tricalciun phosphate, zea mays (corn stach), zinc oxide, zinc stearate

Equate Medicated Body Powder Original

label

MEDICATED BODY  POWDER
menthol powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-724
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.42 g  in 283 g
Inactive Ingredients
Ingredient NameStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
ACACIA (UNII: 5C5403N26O)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
THYMOL (UNII: 3J50XA376E)  
ZINC STEARATE (UNII: H92E6QA4FV)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
ZEA MAYS WHOLE (UNII: 1G5HNE09V8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-724-01283 g in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01709/01/2020
Labeler - Walmart Stores Inc (051957769)

Revised: 4/2024
 
Walmart Stores Inc