Label: GEA COSMETICS LABS HAND AND BODY SANITIZER- benzalkonium chloride 0.13% spray
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Contains inactivated NDC Code(s)
NDC Code(s): 81237-001-10, 81237-001-16 - Packager: Romano Group, 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 January 1, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do Not Use
- When using this product
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- GEA Cosmetics Labs Hand & Body Sanitizer
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INGREDIENTS AND APPEARANCE
GEA COSMETICS LABS HAND AND BODY SANITIZER
benzalkonium chloride 0.13% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81237-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.61 g in 472 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) UREA (UNII: 8W8T17847W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81237-001-16 472 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 2 NDC:81237-001-10 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/01/2021 Labeler - Romano Group, LLC (037493262)