CLOTRIMAZOLE- clotrimazole solution 
Granules Pharmaceuticals Inc.

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Athlete's Foot Solution
Clotrimazole
Topical solution, USP 1%

Active ingredient

Clotrimazole USP, 1%

Purpose

Antifungal

Uses

Cures most
■ Athlete’s foot (tinea pedis)
■ Jock itch (tinea cruris)
■ Ringworm (tinea corporis)

Effectively relieves
■ itching
■ cracking
■ burning
■ discomfort which can accompany these conditions.

Warnings

For external use only.

Ask a doctor before use

• on children under 2 years of age

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• irritation occurs
• there is no improvement within 4 weeks (for athlete’s foot and ringworm) or 2 weeks (for jock itch)

Keep out of reach of children.

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

Directions

Other information

Inactive ingredient

polyethylene glycol

Questions or comments?

call 1-877-770-3183 Mon-Fri 8:00 AM EST to 5:00 PM PST

PRINCIPAL DISPLAY PANEL - Container Label

NDC 70010- 229-54

Clotrimazole
(Topical Solution), USP

1%

Antifungal

For External use only,

not for Opthalmic use.

Keep this and all medications out

of the reach of children.

10 mL (1/3 fl oz)

clotrima-container

PRINCIPAL DISPLAY PANEL - Container Carton Label

NDC 70010- 229-54

*Compare to the active ingredient in

Lotrimin ® AF

Athlete's Foot Solution

Clotrimazole

(Topical Solution),

USP

1%

Antifungal

• Relieves Itching & Burning

• Greaseless, Nonstanining

For External use only,

Not for Ophthalmic use.

Keep this and all medications

out of the reach of children.

10 mL (1/3 fl oz)

clotrima-carton

CLOTRIMAZOLE 
clotrimazole solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70010-229
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65) CLOTRIMAZOLE1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70010-229-5410 mL in 1 BOTTLE; Type 0: Not a Combination Product03/22/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00503/22/2023
Labeler - Granules Pharmaceuticals Inc. (079825711)

Revised: 4/2024
Document Id: 16d347aa-6269-a426-e063-6294a90adcb9
Set id: 1280353c-9f96-557e-e063-6294a90a10f9
Version: 2
Effective Time: 20240424
 
Granules Pharmaceuticals Inc.