Label: SAN-E-FOAM- otc antimicrobial drug products aerosol, foam
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Contains inactivated NDC Code(s)
NDC Code(s): 61924-107-17, 61924-107-34 - Packager: Dermarite Industries LLC
- Category: HUMAN OTC DRUG LABEL
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 January 17, 2020
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- Active Ingredient:
- Purpose:
- Uses:
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- INACTIVE INGREDIENT
- San-E-Foam Package Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
SAN-E-FOAM
otc antimicrobial drug products aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61924-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.67 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61924-107-17 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/12/2012 2 NDC:61924-107-34 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 10/12/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/12/2012 Labeler - Dermarite Industries LLC (883925562) Registrant - Dermarite Industries, LLC (883925562) Establishment Name Address ID/FEI Business Operations Dermarite Industries LLC 883925562 manufacture(61924-107)