Label: UNDECYLENIC ACID- anti-fungal liquid maximum strength liquid
- NDC Code(s): 72446-004-01
- Packager: Hudson Health LLC
- Category: HUMAN OTC DRUG LABEL
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Updated July 20, 2021
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- Active ingredient
For external use only.
Read all warnings and directions. Use only as directed.
- clean the affected area and dry thoroughly
- apply a thin layer of the product over the affecter 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 toeswear 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 conditions persists longer, consult a doctor
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredient
- Principal Display Panel
INGREDIENTS AND APPEARANCE
anti-fungal liquid maximum strength liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72446-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UNDECYLENIC ACID (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N) UNDECYLENIC ACID 7.5 g in 30 g Inactive Ingredients Ingredient Name Strength ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72446-004-01 30 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 09/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 09/01/2018 Labeler - Hudson Health LLC (081276171)