Label: ANTIBACTIERIAL HAND SANITIZER- alcohol liquid
- NDC Code(s): 75857-1103-0
- Packager: Ningbo Dowland Daily Health Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- Active Ingredients
Ethyl Alcohol 62%Close
Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.Close
For external use only.
Flammable. Keep away from fire or flame
Do not apply around eyes. Do not use in ears and mouthClose
- When using this product.
- Other information
- Inactive Ingredients
Water, Triethanolamine, Glycerin, Propylene glycol, Vitamin E, Aloe Vera gel, Carbormer, Fragrance.Close
- Package Labeling
- INGREDIENTS AND APPEARANCE
ANTIBACTIERIAL HAND SANITIZER
ethyl alcohol liquid
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:75857-1103 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER TROLAMINE GLYCERIN PROPYLENE GLYCOL .ALPHA.-TOCOPHEROL ALOE VERA LEAF Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75857-1103-0 30 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/01/2013 Labeler - Ningbo Dowland Daily Health Co., Ltd (421264675)