Label: HANDI-SANI- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76063-738-14, 76063-738-15, 76063-738-16, 76063-738-17, view more76063-738-18, 76063-738-24, 76063-738-55 - Packager: Chromate Industrial Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 April 4, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Box OTC-Active Ingredient Section
- Drug Facts Box OTC-Purpose Section
- Drug Facts Box OTC-Indications and Usage Section
- Drug Facts Box OTC-Warnings Section
- Drug Facts Box OTC-When Using Section
- Drug Facts Box OTC-Stop Use Section
- Drug Facts Box OTC-Keep Out of Reach of Children Section
- Drug Facts Box OTC-Dosage & Administration Section
- Drug Facts Box OTC-Inactive Ingredient Section
- Handi-Sani 6738 4 oz
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INGREDIENTS AND APPEARANCE
HANDI-SANI
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76063-738 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76063-738-14 3785 mL in 1 BOTTLE, PLASTIC 2 NDC:76063-738-15 946 mL in 1 BOTTLE, PLASTIC 3 NDC:76063-738-16 236 mL in 1 BOTTLE, PLASTIC 4 NDC:76063-738-17 532 mL in 1 BOTTLE, PLASTIC 5 NDC:76063-738-18 50 mL in 1 BOTTLE, PLASTIC 6 NDC:76063-738-24 118 mL in 1 BOTTLE, PLASTIC 7 NDC:76063-738-55 208200 mL in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/01/2011 Labeler - Chromate Industrial Corporation (061955621) Registrant - ABC Compounding Co., Inc. (003284353) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture
