LOTRIMIN DAILY PREVENTION DEO- tolnaftate aerosol, powder

Lotrimin Daily Prevention Deo by

Drug Labeling and Warnings

Lotrimin Daily Prevention Deo 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

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.

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.
do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF

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, isobutane, PEG-12-Buteth-16, SD alcohol 40B (10.5% v/v), talc

QUESTIONS

Questions? 1-866-360-3266

Display can 160 grams

Lotrimin®AF

TOLNAFTATE ANTIFUNGAL

deodorant powder spray

DAILY PREVENTION

clinically proven to

prevent most

athlete's foot

• stops the growth of most athlete's foot fungus
• instantly cools and dries feet
• fights odor all day

NET WT 160 g (5.6 OZ)

INGREDIENTS AND APPEARANCE

LOTRIMIN DAILY PREVENTION DEO 
tolnaftate aerosol, powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0010
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
ISOBUTANE (UNII: BXR49TP611)
ALCOHOL (UNII: 3K9958V90M)
TALC (UNII: 7SEV7J4R1U)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PPG-12-BUTETH-16 (UNII: 58CG7042J1)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0010-1	160 g in 1 CAN; Type 0: Not a Combination Product	02/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	02/14/2020

Labeler - Bayer HealthCare LLC. (112117283)