Label: DOCTOR INKS HAND SANITIZER- benzalkonium chloride liquid
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NDC Code(s):
71884-201-01,
71884-201-02,
71884-201-03,
71884-201-04, view more71884-201-05, 71884-201-06
- Packager: Enviro Specialty Chemicals 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 February 14, 2023
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- Drug Facts
- Active Ingredient:
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- Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
Long-lasting, alcohol-free protection from germs
Formulated and enhanced with Zetrisil®
Kills 99.9% of Germs
Alcohol Free
Contains Soothing Aloe Vera
Fast-acting
15-Second FormulaFoaming Pump Top
Distributed by:
ESC Brands, LLC.
1060 Blue Prince Road
Bluefield, WV 24701
www.doctor-ink.comFORMULATED IN THE USA
MADE IN CHINA
- Packaging
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INGREDIENTS AND APPEARANCE
DOCTOR INKS HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71884-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) LAURETH-4 (UNII: 6HQ855798J) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71884-201-01 58 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/01/2022 2 NDC:71884-201-02 118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/01/2022 3 NDC:71884-201-03 244 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/01/2022 4 NDC:71884-201-04 473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 09/01/2022 5 NDC:71884-201-05 1182 mL in 1 BAG; Type 0: Not a Combination Product 09/01/2022 6 NDC:71884-201-06 3785 mL in 1 JUG; Type 0: Not a Combination Product 09/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/01/2022 Labeler - Enviro Specialty Chemicals Inc (202621850)