OTC Medication Information: Blistex Odor Eaters Medicated Foot

BLISTEX ODOR EATERS MEDICATED FOOT- menthol, unspecified form powder
Blistex Inc.

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.

Drug Facts

Active ingredient

Menthol 1.0% (w/w)

Purpose

External Analgesic

Uses

  • For the temporary relief of pain and itching associated with minor skin irritations

Warnings

For external use only

When using this product avoid contact with eyes

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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: consult a physician.
  • Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. For best results apply to affected areas up to 3 or 4 times daily. Sprinkle inside shoes and/or socks for maximum freshness.

Inactive ingredients

avena sativa kernel flour (collodial oatmeal), benzethonium chloride, eucalyptus globulus leaf oil, gum arabic, sodium bicarbonate, sodium polyacrylate (crosslinked), tricalcium phosphate, zea mays (corn) starch

PRINCIPAL DISPLAY PANEL — 142 g Bottle Label

NEW!

NDC 10157-3101-1

Odor-
Eaters®

3
ADVANCED
ODOR/WETNESS
FIGHTERS

MEDICATED FOOT POWDER

MENTHOL 1% W/W EXTERNAL ANALGESIC

Controls Odor & Wetness + Relieves Itching & Irritation

ALL-DAY EFFECTIVENESS

STOPS ODOR

GUARANTEED!

Net Wt.
5 oz. (142 g)

Principal Display Panel -- 142 g Bottle Label
(click image for full-size original)
BLISTEX ODOR EATERS MEDICATED FOOT
menthol, unspecified form powder
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-3101
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL, UNSPECIFIED FORM (MENTHOL, UNSPECIFIED FORM) MENTHOL, UNSPECIFIED FORM 1 g in 100 g
Inactive Ingredients
Ingredient Name Strength
OATMEAL
BENZETHONIUM CHLORIDE
EUCALYPTUS OIL
ACACIA
SODIUM BICARBONATE
SODIUM POLYACRYLATE (8000 MW)
TRICALCIUM PHOSPHATE
STARCH, CORN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10157-3101-1 142 g in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 02/01/2015
Labeler — Blistex Inc. (005126354)
Establishment
Name Address ID/FEI Operations
Blistex Inc. 005126354 MANUFACTURE (10157-3101)

Revised: 01/2015 Blistex Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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