BLADE FOR MEN MEDICATED BODY POWDER- menthol powder 
Davion, Inc.

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Blade for Men Medicated Body Powder

Active Ingredient

Menthol 0.15%

Purpose

External Analgesic

Uses

Temporary relief of pain and itch associate with:

  • minor cuts
  • sunburn
  • insect bites
  • scrapes
  • minor burns
  • minor skin irritations

Warning

  • For external use only
  • Avoid contact with eyes

Stop use and ask a doctor if

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

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a poison control center right away.

Directions

Remove seal beneath cap before first use. Do not use if seal is broken

  • adults and children 2 years and older - apply freely upto 3 or 4 times daily
  • children under 2 years - ask a doctor

For best results, dry skin throughly before applying

Inactive ingredients

Zea Mays (Corn) Starch, Tricalcium Phosphate,  Sodium Bicarbonate, Benzethonium Chloride, Eucalyptol, Peppermint Oil

Principal Display Panel

NDC 42669-282-01

BLADE FOR MEN

MEDICATED BODY POWDER

EXTERNAL ANALGESIC

TALC FREE

PAIN RELEIVING POWDER

ABSORBS MOISTURE

ITCH RELEIVING

PARABEN & PTHALATE FREE

Compare to the active ingredient in Gold Bond Medicated Body Powder*

CVS pharmacy

NET WT 10 OZ (283g)

Label

BLADE FOR MEN MEDICATED BODY POWDER 
menthol powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42669-282
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
EUCALYPTOL (UNII: RV6J6604TK)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
ZINC STEARATE (UNII: H92E6QA4FV)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
STARCH, CORN (UNII: O8232NY3SJ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42669-282-01283 g in 1 BOTTLE; Type 0: Not a Combination Product01/30/201802/03/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/30/201802/03/2020
Labeler - Davion, Inc. (174542928)
Registrant - Davion, Inc. (174542928)

Revised: 1/2024
Document Id: 0e246ca1-ce35-584a-e063-6394a90a1212
Set id: 13c4edf1-47ca-4176-8e8d-e26153ec4036
Version: 3
Effective Time: 20240104
 
Davion, Inc.