Label: ANTIBACTERIAL HAND SANITIZER- ethyl alcohol gel
-
NDC Code(s):
70412-110-15,
70412-110-29,
70412-110-30,
70412-110-40, view more70412-110-45, 70412-110-53, 70412-110-58, 70412-110-59, 70412-110-60, 70412-110-75, 70412-110-88
- Packager: Zhejiang Ayan Biotech Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses:
- Warnings:
- Directions:
- Other Information:
- Inactive Ingredients
- Package Labeling:
- Hand Sanitizer 40mL/1.35oz 70412-110-40
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70412-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 620 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70412-110-15 1 in 1 BOX 01/19/2016 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:70412-110-29 1 in 1 BOX 01/19/2016 2 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:70412-110-30 1 in 1 BOX 01/19/2016 3 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:70412-110-45 1 in 1 BOX 01/19/2016 4 45 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:70412-110-53 1 in 1 BOX 01/19/2016 5 53 mL in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:70412-110-58 1 in 1 BOX 01/19/2016 6 58 mL in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:70412-110-59 1 in 1 BOX 01/19/2016 7 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:70412-110-60 1 in 1 BOX 01/19/2016 8 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 9 NDC:70412-110-75 1 in 1 BOX 01/19/2016 9 75 mL in 1 BOTTLE; Type 0: Not a Combination Product 10 NDC:70412-110-88 1 in 1 BOX 01/19/2016 10 88 mL in 1 BOTTLE; Type 0: Not a Combination Product 11 NDC:70412-110-40 40 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/19/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/19/2016 Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)