Label: SANI LUXE FOAMING HAND SANITIZER ALCOHOL FREE- benzalkonium chloride liquid
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NDC Code(s):
71489-006-01,
71489-006-02,
71489-006-03,
71489-006-04, view more71489-006-05, 71489-006-06, 71489-006-07, 71489-006-08, 71489-006-09, 71489-006-10, 71489-006-11, 71489-006-12, 71489-006-13, 71489-006-14, 71489-006-15, 71489-006-16
- Packager: Celeste Industries Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- 236 ml Bottle Label
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INGREDIENTS AND APPEARANCE
SANI LUXE FOAMING HAND SANITIZER ALCOHOL FREE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71489-006 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) TRIETHYLENE GLYCOL (UNII: 3P5SU53360) GLYCERETH-26 (UNII: NNE56F2N14) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR) DMDM HYDANTOIN (UNII: BYR0546TOW) TROLAMINE (UNII: 9O3K93S3TK) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71489-006-01 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/28/2019 2 NDC:71489-006-02 56 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/25/2020 3 NDC:71489-006-03 177 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/20/2020 4 NDC:71489-006-04 284 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/20/2020 5 NDC:71489-006-05 355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/20/2020 6 NDC:71489-006-06 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/20/2020 7 NDC:71489-006-07 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/25/2020 8 NDC:71489-006-08 177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/25/2020 9 NDC:71489-006-09 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/25/2020 10 NDC:71489-006-10 284 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/25/2020 11 NDC:71489-006-11 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/25/2020 12 NDC:71489-006-12 3785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/25/2020 13 NDC:71489-006-13 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/30/2020 14 NDC:71489-006-14 946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/30/2020 15 NDC:71489-006-15 530 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/14/2020 16 NDC:71489-006-16 530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/28/2019 Labeler - Celeste Industries Corporation (047795034)