WELMATE CLOTRIMAZOLE TOPICAL SOLUTION- clotrimazole liquid

WELMATE Clotrimazole Topical Solution by

Drug Labeling and Warnings

WELMATE Clotrimazole Topical Solution by is a Otc medication manufactured, distributed, or labeled by YYBA CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

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

• This product is not effective on the scalp or nails. For best results, follow directions and continue treatment for length of time indicated. For athlete's foot and ringworm: use daily for 4 weeks. For jock itch: use daily for 2 weeks.
• clean the affected area and dry thoroughly
• apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
• supervise children in the use of this product.

For athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes; change shoes and socks at least once daily.

Other information

Store at 15° to 30°C (59° to 86°F)

Inactive ingredient

polyethylene glycol 400

Questions?

call 866-933-6337

Package Labeling:

INGREDIENTS AND APPEARANCE

WELMATE CLOTRIMAZOLE TOPICAL SOLUTION 
clotrimazole liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73581-449
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73581-449-00	1 in 1 BOX	02/19/2024
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	02/19/2024

Labeler - YYBA CORP (006339772)