Label: ANTI-BACTERIAL HAND EUCALYPTUS MINT- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 62670-6009-2 - Packager: Bath & Body Works, 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 December 9, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENTS
INACTIVE INGREDIENTS: Water (Aqua, Eau), Fragrance (Parfum), PEG-12 Dimethicone, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Butylene Glycol, Aloe Barbadensis Leaf Juice, Propylene Glycol, Tocopheryl Acetate, Cocos Nucifera (Coconut) Fruit Extract, Honey Extract (Mel, Extrait de miel), Olea Europaea (Olive) Fruit Extract, Ext. Violet 2 (CI 60730).
- COMPANY INFORMATION
- PRODUCT PACKAGING
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INGREDIENTS AND APPEARANCE
ANTI-BACTERIAL HAND EUCALYPTUS MINT
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 72 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62670-6009-2 56 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 12/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/09/2020 Labeler - Bath & Body Works, Inc. (878952845)