Label: AVANT ORIGINAL INSTANT HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 68306-101-01, 68306-101-02, 68306-101-04, 68306-101-05, view more68306-101-06, 68306-101-07 - Packager: B4 Ventures 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 October 5, 2010
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- Official Label (Printer Friendly)
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Bio-Based Hand Sanitizer
Avant Original Instant Hand Sanitizer is bio-based and part of B4 Brands' family of environmentally sensitive products. Avant Original contains 60% grain based ethanol and other natural ingredients, making it more environmentally sensitive than petroleum based products.
Learn more about our products at www.b4brands.com
- ACTIVE INGREDIENT
- Purpose
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Warnings:
- FOR EXTERNAL USE ONLY.
- FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
- Keep away from eyes. In case of eye contact, flush thoroughly with water and then seek medical advice.
- If swallowed, drink large amounts of water and seek medical attention.
- Avoid contact with face and broken skin. If contact occurs, flush with water.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
- Other Ingredients:
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
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INGREDIENTS AND APPEARANCE
AVANT ORIGINAL INSTANT HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68306-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Propylene Glycol (UNII: 6DC9Q167V3) Trolamine (UNII: 9O3K93S3TK) Carbomer 1342 (UNII: 809Y72KV36) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68306-101-04 80 mL in 1 BOTTLE, DISPENSING 2 NDC:68306-101-06 500 mL in 1 BOTTLE, PUMP 3 NDC:68306-101-07 1000 mL in 1 POUCH 4 NDC:68306-101-05 251 mL in 1 BOTTLE, PUMP 5 NDC:68306-101-01 3784 mL in 1 BOTTLE 6 NDC:68306-101-02 208120 mL in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/05/2010 Labeler - B4 Ventures LLC (133582853) Registrant - B4 Ventures LLC (133582853)