BLADE FOR MEN MEDICATED BODY POWDER- menthol powder

Blade for Men Medicated Body Powder by

Drug Labeling and Warnings

Blade for Men Medicated Body Powder by is a Otc medication manufactured, distributed, or labeled by Davion, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

BLADE FOR MEN MEDICATED BODY POWDER 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42669-282
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42669-282-01	283 g in 1 BOTTLE; Type 0: Not a Combination Product	01/30/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/30/2018

Labeler - Davion, Inc. (174542928)

Registrant - Davion, Inc. (174542928)

Establishment
Name	Address	ID/FEI	Business Operations
Davion, Inc.		174542928	manufacture(42669-282)