Label: SALLY HANSEN NO MORE FUNGUS- undecylenic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66184-151-01, 66184-151-02 - Packager: Coty US 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 October 19, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
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Directions
Use daily for 4 weeks. This product is not effective on the scalp or nails.
- wash 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, veniltated shoes
- change shoes and socks at least once daily
- Other Information
- Inactive ingredients
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Questions or comments?
To report a serious adverse event and for informaiton or comments on this product call us at 1-800-953-5080
9:00AM-5:00PM EST or visit www.sallyhansen.com
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SALLY HANSEN NO MORE FUNGUS
undecylenic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66184-151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UNDECYLENIC ACID (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N) UNDECYLENIC ACID 0.23125 g in 39.01 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL DICAPRYLATE (UNII: 581437HWX2) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+)- (UNII: F4VNO44C09) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66184-151-02 1 in 1 BOX 01/01/2012 1 NDC:66184-151-01 39 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 final part333C 01/01/2012 Labeler - Coty US LLC (039056361) Establishment Name Address ID/FEI Business Operations Kolmar Laboratories Inc. 001535103 manufacture(66184-151)