LOTRIMIN DAILY SWEAT AND ODOR CONTROL- topical starch powder

Lotrimin Daily Sweat and Odor Control by

Drug Labeling and Warnings

Lotrimin Daily Sweat and Odor Control by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Topical starch 83.7%

PURPOSE

Purpose

Skin Protectant

Use

Use

temporarily protects and helps relieve minor skin irritation

WARNINGS

Warnings

For external use only

Do not use on broken skin.

When using this product

Do not get into eyes

Keep away from face and mouth to avoid breathing it

Stop use and ask a doctor if

• Condition worsens
• Symptoms last more than 7 days or clear up and occur again within a few days

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

Directions

Directions

Apply as needed

INACTIVE INGREDIENT

Inactive ingredients

benzethonium chloride;camphor (synthetic);eucalyptus oil;kaolin;lemon oil;zinc oxide

Questions

Questions? 1-866-360-3266

Package display

LOTRIMIN

TOPICAL STARCH SKIN PROTECTANT

medicated foot powder

DAILY SWEAT

& ODOR CONTROL

6 odor-fighting

ingredients to control odor

• super sweat absorbent powder
• relieves irritation
• talc-free

NET WT 177 G (6.25 OZ)

INGREDIENTS AND APPEARANCE

LOTRIMIN DAILY SWEAT AND ODOR CONTROL 
topical starch powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ)	STARCH, CORN	837 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ZINC OXIDE (UNII: SOI2LOH54Z)
LEMON OIL (UNII: I9GRO824LL)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
KAOLIN (UNII: 24H4NWX5CO)
EUCALYPTUS OIL (UNII: 2R04ONI662)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0012-1	177 g in 1 BOTTLE; Type 0: Not a Combination Product	02/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	02/17/2020

Labeler - Bayer HealthCare LLC. (112117283)