Label: CARE AND CO HAND SANITIZER- benzalkonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 80755-001-01, 80755-001-02 - Packager: CARE AND COMPANY USA. LLC
- 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 3, 2021
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- Drug Facts
- Active ingredient
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- Inactive ingredients
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- Package Labeling:59ml
- Package Labeling:118ml
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INGREDIENTS AND APPEARANCE
CARE AND CO HAND SANITIZER
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80755-001 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 GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80755-001-01 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2020 2 NDC:80755-001-02 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/15/2020 Labeler - CARE AND COMPANY USA. LLC (107409020)