Label: NELLIES HAND SANITIZER- benzalkonium chloride liquid
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NDC Code(s):
73126-006-01,
73126-006-02,
73126-006-03,
73126-006-04, view more73126-006-05, 73126-006-06, 73126-006-07
- Packager: LAB-CLEAN, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 April 26, 2022
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Warnings
- Keep out of reach of children.
- Uses
- Directions
- Inactive Ingredients
- Package
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INGREDIENTS AND APPEARANCE
NELLIES HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73126-006 Route of Administration TOPICAL 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) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) GLYCERETH-17 COCOATE (UNII: 3057VPT0KC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73126-006-01 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 2 NDC:73126-006-02 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 3 NDC:73126-006-03 710 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 4 NDC:73126-006-04 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 5 NDC:73126-006-05 3000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 6 NDC:73126-006-06 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 7 NDC:73126-006-07 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/22/2020 04/20/2024 Labeler - LAB-CLEAN, INC (199822219) Establishment Name Address ID/FEI Business Operations LAB-CLEAN, INC 199822219 manufacture(73126-006)