TOLNAFTATE- jock itch powder aerosol, spray

Tolnaftate by

Drug Labeling and Warnings

Tolnaftate by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

​Uses

• cures most jock itch (tinea cruris)
• relieves itching, burning and chafing associated with jock itch

​Warnings

​ For external use only.

​Flammable:

Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

​When using this product

• avoid contact with eyes
• use only as directed

​Stop use and ask a doctor if

• irritation occurs
• no improvement within 2 weeks

​Do not use

• on children under 2 years of age unless directed by a doctor.

​Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

​Directions

• wash affected area and dry thoroughly
• shake can well and spray a thin layer over affected area twice daily (morning and night)
• supervise children in the use of this product
• use daily for 2 weeks; if conditions persists, consult a doctor
• if nozzle clogs, clean with a pin

​Other information

store between 20º and 30ºC (68º and 86ºF)

​Inactive ingredient

BHT, isobutane, kaolin, PPG-12-buteth-16, SD alcohol 40-B, zea mays (corn) starch

Questions?

Call 1-866-964-0939

Principal Display Panel

Compare to the active

ingredient, in Tinactin

Jock Itch Powder Spray

ANTIFUNGAL

JOCK ITCH

POWDER SPRAY

tolnaftate 1%

Cures most jock itch
Relieves itching, chafing & burning
Talc-free

NET WT

4.6 OZ (130 g)

INGREDIENTS AND APPEARANCE

TOLNAFTATE 
jock itch powder aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0782
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	1.3 g  in 130 g

Inactive Ingredients
Ingredient Name	Strength
KAOLIN (UNII: 24H4NWX5CO)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
ISOBUTANE (UNII: BXR49TP611)
PPG-12-BUTETH-16 (UNII: 58CG7042J1)
ALCOHOL (UNII: 3K9958V90M)
ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0782-4	130 g in 1 CAN; Type 0: Not a Combination Product	03/15/2021	03/31/2028

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/15/2021	03/31/2028

Labeler - Rite Aid Corporation (014578892)