LOTRIMIN DAILY PREVENT DEODORANT- tolnaftate aerosol, powder

Lotrimin by

Drug Labeling and Warnings

Lotrimin 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

(To Deliver)Tolnaftate 1%

PURPOSE

Purpose

Antifungal

Use

Use

clinically proven to prevent most athlete’s foot with daily use

WARNINGS

Warnings

For external use only

Flammable: Do not use near heat, flame, or while smoking

Do not use on children under 2 years of age unless directed by a doctor

When using this product

• avoid contact with the eyes
• use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
• contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120ºF.

Stop use and ask a doctor if irritation occurs.

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

Directions

Directions

• to prevent athlete’s foot, wash the feet and dry thoroughly.
• shake can well and spray a thin layer of the product on the feet once or twice daily (morning and/or night).
• supervise children in the use of this product.
• pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Other information

Other Information

store between 20º to 25ºC (68º– 77ºF)

INACTIVE INGREDIENT

Inactive Ingredients

butylated hydroxytoluene, fragrance, hydroxypropyl cellulose, isobutane, kaolin, magnesium stearate, PPG-12-Buteth-16, SD alcohol 40B (9% w/w), zea mays (corn) starch

QUESTIONS

Questions?1-866-360-3266 or visit us at www.lotrimin.com

Display can 160 grams

INGREDIENTS AND APPEARANCE

LOTRIMIN  DAILY PREVENT DEODORANT
tolnaftate aerosol, powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0136
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ALCOHOL (UNII: 3K9958V90M)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
PPG-12-BUTETH-16 (UNII: 58CG7042J1)
ISOBUTANE (UNII: BXR49TP611)
KAOLIN (UNII: 24H4NWX5CO)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0136-1	160 g in 1 CAN; Type 0: Not a Combination Product	03/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/01/2024

Labeler - Bayer HealthCare LLC. (112117283)