Label: ANTISEPTIQUE ADVANCE STRENGTH- alcohol spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 72138-420-16, 72138-420-20, 72138-420-40, 72138-420-60 - Packager: Hubot Healthcare LLC
- Category: HUMAN OTC DRUG LABEL
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 25, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purposes
- Uses
- Warnings
- Directions
- Other Information
- Inactive Ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL - 59 ML Bottle Label
-
INGREDIENTS AND APPEARANCE
ANTISEPTIQUE ADVANCE STRENGTH
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72138-420 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Hydrogen Peroxide (UNII: BBX060AN9V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72138-420-20 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/20/2020 2 NDC:72138-420-40 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/20/2020 3 NDC:72138-420-60 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/20/2020 4 NDC:72138-420-16 472 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 03/19/2020 Labeler - Hubot Healthcare LLC (081084880)