H-E-B MEDICATED CORN STARCH FOOT POWDER- menthol powder

H-E-B Medicated Corn Starch Foot Powder by

Drug Labeling and Warnings

H-E-B Medicated Corn Starch Foot 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 1.0%

Purpose

External Analgesic

Uses

Temporary relief of pain and itch associate with:

• Minor Cuts
• Sunburn
• Insect Bites
• Scrapes
• Minor Burns
• Minor Skin Irritations

Warnings

• 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

• 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, Eucalyptus Oil, Peppermint Oil.

PRINCIPAL DISPLAY PANEL

NDC: 42669-218-10

Compare to Gold Bond ® Medicated Foot Powder active ingredient*

H-E-B Medicated Corn Starch Foot Powder

TRIPLE RELIEF FORMULA

• Controls Odor
• Absorbs Moisture
• Relieves Itching

Talc-Free

NET WT. 10 OZ (283g)

INGREDIENTS AND APPEARANCE

H-E-B MEDICATED CORN STARCH FOOT POWDER 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42669-218
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
EUCALYPTUS OIL (UNII: 2R04ONI662)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42669-218-10	283 g in 1 BOTTLE; Type 0: Not a Combination Product	08/22/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/22/2018

Labeler - Davion, Inc (174542928)

Registrant - Davion, Inc (174542928)

Establishment
Name	Address	ID/FEI	Business Operations
Davion, Inc		174542928	manufacture(42669-218)