Label: MOISTURIZING FOAM HAND SANITIZER- alcohol liquid
- NDC Code(s): 74401-500-12, 74401-500-33, 74401-500-40, 74401-500-64
- Packager: Volu-Sol
- 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 16, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
MOISTURIZING FOAM HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74401-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 74.3 mL in 100 mL Inactive Ingredients Ingredient Name Strength PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N) 0.165 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 1.35 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL in 100 mL WATER (UNII: 059QF0KO0R) 2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V) 0.165 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74401-500-33 300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/30/2020 2 NDC:74401-500-12 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 3 NDC:74401-500-40 400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/30/2020 4 NDC:74401-500-64 1893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Volu-Sol (050173424) Registrant - Volu-Sol (050173424) Establishment Name Address ID/FEI Business Operations Volu-Sol 050173424 manufacture(74401-500)