PROCLEARZ PROFESSIONAL FUNGAL SHIELD- tolnaftate liquid

Proclearz Professional Fungal Shield by

Drug Labeling and Warnings

Proclearz Professional Fungal Shield by is a Otc medication manufactured, distributed, or labeled by Rooftop Consumer health, inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Tolnaftate 1%

Purpose

Antifungal

Uses

• cures most athlete's foot (tinea pedis) and ringworm (tinea corporis)
• helps prevent most athlete's foot from recurring when used daily
• relieves itching, scaling, cracking, burning, and redness

Warnings

For external use only

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

Extremely flammable keep away from fire or flame

When using this product

• avoid contact with the eyes.
• if contact occurs rinse thoroughly with water

Stop use and ask a doctor if

• irritation occurs or if there is no improvement within 4 weeks

Keep out of reach of children.

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

Directions

• shake well before using
• wash affected area and dry thoroughly
• apply a thin layer of the product over affected area (around the nails and underneath nail tips) twice daily 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 and change shoes and socks at least once daily
• for athlete's foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor
• this product is not effective on the scalp or nails

Other information

• store at room temperature 15°-30°C (59°-86°F)

Inactive ingredients

Acetone, Aloe Barbadensis Leaf Powder, Propylene Glycol, Tocopherol (Vitamin E), Water

Questions or comments?

www.rooftopch.com
cservice@rooftopch.com

Package Labeling:

INGREDIENTS AND APPEARANCE

PROCLEARZ PROFESSIONAL FUNGAL SHIELD 
tolnaftate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29784-184
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 mL

Inactive Ingredients
Ingredient Name	Strength
ACETONE (UNII: 1364PS73AF)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29784-184-01	1 in 1 BOX	03/01/2025
1		45 mL in 1 BOTTLE, GLASS; 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	03/01/2025

Labeler - Rooftop Consumer health, inc (107570900)