Label: VAX-MAN ANTISEPTIC HAND WIPES- alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79566-001-01, 79566-001-02, 79566-001-03, 79566-001-04, view more79566-001-05, 79566-001-06, 79566-001-07, 79566-001-08, 79566-001-09, 79566-001-10, 79566-001-11 - Packager: Vaxman Group 2015 Ltd.
- 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 July 10, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Company Information
- Product Packaging - 200 wipe canister
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INGREDIENTS AND APPEARANCE
VAX-MAN ANTISEPTIC HAND WIPES
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79566-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) LACTIC ACID (UNII: 33X04XA5AT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79566-001-02 50 in 1 POUCH 07/10/2020 1 240 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:79566-001-04 100 in 1 POUCH 07/10/2020 2 480 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:79566-001-03 80 in 1 POUCH 07/10/2020 3 384 mL in 1 POUCH; Type 0: Not a Combination Product 4 NDC:79566-001-01 1 in 1 PACKET 07/10/2020 4 4.8 mL in 1 PACKET; Type 0: Not a Combination Product 5 NDC:79566-001-05 80 in 1 CANISTER 07/10/2020 5 150 mL in 1 CANISTER; Type 0: Not a Combination Product 6 NDC:79566-001-06 100 in 1 CANISTER 07/10/2020 6 150 mL in 1 CANISTER; Type 0: Not a Combination Product 7 NDC:79566-001-07 140 in 1 CANISTER 07/10/2020 7 210 mL in 1 CANISTER; Type 0: Not a Combination Product 8 NDC:79566-001-08 200 in 1 CANISTER 07/10/2020 8 420 mL in 1 CANISTER; Type 0: Not a Combination Product 9 NDC:79566-001-09 400 in 1 CONTAINER 07/10/2020 9 840 mL in 1 CONTAINER; Type 0: Not a Combination Product 10 NDC:79566-001-10 500 in 1 CONTAINER 07/10/2020 10 1050 mL in 1 CONTAINER; Type 0: Not a Combination Product 11 NDC:79566-001-11 750 in 1 CONTAINER 07/10/2020 11 1575 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/10/2020 Labeler - Vaxman Group 2015 Ltd. (531964346)
