Label: PERSONAL CARE ANTIFUNGAL- tolnaftate spray
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Contains inactivated NDC Code(s)
NDC Code(s): 29500-0035-3 - Packager: Personal Care Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 1, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active ingredient
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
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Directions
- wash affected area and dry thoroughly
- shake can well and spray a this layer over affected area twice daily (morning and night)
- supervise children in the use of this product
- for athlete's foot: pay special attention to the spaces between the toes, wear well-fitting, ventilated shoes and change shoes and socks at least once day.
- use daily for 4 weeks; if condition persists longer, consult a doctor
- to prevent athlete's foot, apply once or twice daily (morning and night)
- in case of clogging, clean nozzle with a pin
- Other information
- Inactive ingredients
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ANTI FUNGAL POWDER SPRAY Label
PERSONAL CARE®
ANTIFUNGAL POWDER SPRAY
For Athlete's FootTOLNAFTATE 1%
*Compare to the Active Ingredients in Tinactin®
Cures and Prevents Most Athlete's Foot
Relieves Itching and Burning
*This product is not manufactured ir distributed by Schering-Plough HealthCare Products, Inc., owner of the registered trademark Tinactin®
Distributed by: Personal Care Products, Inc. Bingham Farms, MI 48025-3463
Made in China
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INGREDIENTS AND APPEARANCE
PERSONAL CARE ANTIFUNGAL
tolnaftate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:29500-0035 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ISOBUTANE (UNII: BXR49TP611) PROPANE (UNII: T75W9911L6) BUTANE (UNII: 6LV4FOR43R) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29500-0035-3 100 g in 1 CANISTER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 05/21/2010 Labeler - Personal Care Products, Inc. (966155082)