Label: ANTI BACTERIAL HAND SANITIZER- ethyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 49852-069-30, 49852-069-40 - Packager: Tri-Coastal Design Company Inc.
- 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 July 4, 2014
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Keep out of reach of children
- Directions
- Other Information
- Inactive Ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
ANTI BACTERIAL HAND SANITIZER
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49852-069 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength SULISOBENZONE (UNII: 1W6L629B4K) FD&C RED NO. 40 (UNII: WZB9127XOA) D&C RED NO. 33 (UNII: 9DBA0SBB0L) GLYCERIN (UNII: PDC6A3C0OX) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TOCOPHEROL (UNII: R0ZB2556P8) JOJOBA OIL (UNII: 724GKU717M) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49852-069-30 30 mL in 1 BOTTLE, PLASTIC 2 NDC:49852-069-40 40 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/15/2011 Labeler - Tri-Coastal Design Company Inc. (609734900)