Label: TING- tolnaftate cream
- NDC Code(s): 63736-051-01
- Packager: Insight Pharmaceuticals LLC
- 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 March 1, 2018
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- 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 use daily for 4 weeks. If condition persists longer, consult a doctor.
- Pay special attention to the spaces between the toes.
- Wear well-fitting, ventilated shoes and change shoes and socks at least once daily.
- To prevent athlete's foot, clean feet and dry thoroughly, then apply a thin layer of product to feet once or twice daily (morning and/or night) following the above directions.
For ringworm use daily for 4 weeks. If condition persists longer, consult a doctor.
For jock itch use daily for 2 weeks. If condition persists longer, consult a doctor.
This product is not effective on the scalp or nails.
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
TING
tolnaftate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-051 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 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-051-01 1 in 1 BOX 06/08/2009 1 14 g in 1 TUBE; 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 06/08/2009 Labeler - Insight Pharmaceuticals LLC (055665422)