Label: ANTISEPTIQUE- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72138-480-06, 72138-480-16, 72138-480-32 - Packager: Hubot Healthcare 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 March 18, 2020
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purposes
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- Other Information
- Inactive Ingredients
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- PRINCIPAL DISPLAY PANEL - 473 ML Bottle Label
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INGREDIENTS AND APPEARANCE
ANTISEPTIQUE
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72138-480 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62.5 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Dimethicone PEG-7 Isostearate (UNII: JVS3399FNW) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) Tocopherol (UNII: R0ZB2556P8) Aloe Vera Leaf (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72138-480-06 177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/12/2020 2 NDC:72138-480-16 473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/12/2020 3 NDC:72138-480-32 946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/12/2020 Labeler - Hubot Healthcare LLC (081084880)