Label: INSTANT HAND SANITIZER- alcohol gel
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NDC Code(s):
61010-1111-0,
61010-1111-1,
61010-1111-3,
61010-1111-4, view more61010-1111-5, 61010-1111-6, 61010-1111-7, 61010-1111-8, 61010-1111-9
- Packager: Safetec of America, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 12, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL – 1.9 L Bottle Label
- PRINCIPAL DISPLAY PANEL – 0.0570 fl. oz. box
- PRINCIPAL DISPLAY PANEL – 0.0570 fl. oz. packet
- Principal Display Panel – 2.0 FL OZ Bottle Panel
- Principal Display Panel – 4.0 FL OZ Bottle Panel
- Principal Display Panel – 8.0 FL OZ Bottle Panel
- Principal Display Panel – 16.0 FL OZ Bottle Panel
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INGREDIENTS AND APPEARANCE
INSTANT HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61010-1111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 540.26 g in 1 L Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61010-1111-7 1.9 L in 1 BOTTLE; Type 0: Not a Combination Product 12/16/2010 2 NDC:61010-1111-5 0.8 L in 1 BOX; Type 0: Not a Combination Product 12/16/2010 3 NDC:61010-1111-9 1 L in 1 BOX; Type 0: Not a Combination Product 12/16/2010 4 NDC:61010-1111-3 100 in 1 BOX 12/16/2010 4 0.0037 L in 1 PACKET; Type 0: Not a Combination Product 5 NDC:61010-1111-8 100 in 1 BOX 12/16/2010 5 0.00168 L in 1 PACKET; Type 0: Not a Combination Product 6 NDC:61010-1111-0 0.059 L in 1 BOTTLE; Type 0: Not a Combination Product 12/16/2010 7 NDC:61010-1111-1 0.118 L in 1 BOTTLE; Type 0: Not a Combination Product 12/16/2010 8 NDC:61010-1111-6 0.237 L in 1 BOTTLE; Type 0: Not a Combination Product 12/16/2010 9 NDC:61010-1111-4 0.473 L in 1 BOTTLE; Type 0: Not a Combination Product 12/16/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 12/16/2010 Labeler - Safetec of America, Inc. (874965262) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc. 874965262 manufacture(61010-1111)