VAX-MAN ANTISEPTIC HAND WIPES- alcohol cloth 
Vaxman Group 2015 Ltd.

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.

----------

Vax-Man Antiseptic Hand Wipes

Drug Facts

Active ingredients

Alcohol 70% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only.

Flammable. Keep away from heat or flame.

Do not use

as a diaper wipe

When using this product

avoid contact with eyes. If contact occurs, flush thoroughly with water.

Discontinue use

if irritation or redness develops. If condition persists for more than 72 hours contact a doctor.

Keep out of reach of children

unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Store in a cool, dry place, away from direct sunlight

Contact: 415 Ocean Parkway Apt 2g. Brooklyn NY 11218

Inactive ingredients

Water, Aloe Barbadensis Leaf Juice, Glycerin, Potassium Sorbate, Sodium Benzoate, Fragrance, Lactic Acid.

Company Information

Vaxman Group 2015 Ltd

Haifa Israel

vaxmangroup@gmail.com

www.vaxmangroupcom

Made in Israel

Product Packaging - 200 wipe canister

Vax-Man

Antiseptic Hand Wipes

For a better world

70% Alcohol

200 WIPES

vaxman wipes

VAX-MAN ANTISEPTIC HAND WIPES 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79566-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79566-001-0250 in 1 POUCH07/10/2020
1240 mL in 1 POUCH; Type 0: Not a Combination Product
2NDC:79566-001-04100 in 1 POUCH07/10/2020
2480 mL in 1 POUCH; Type 0: Not a Combination Product
3NDC:79566-001-0380 in 1 POUCH07/10/2020
3384 mL in 1 POUCH; Type 0: Not a Combination Product
4NDC:79566-001-011 in 1 PACKET07/10/2020
44.8 mL in 1 PACKET; Type 0: Not a Combination Product
5NDC:79566-001-0580 in 1 CANISTER07/10/2020
5150 mL in 1 CANISTER; Type 0: Not a Combination Product
6NDC:79566-001-06100 in 1 CANISTER07/10/2020
6150 mL in 1 CANISTER; Type 0: Not a Combination Product
7NDC:79566-001-07140 in 1 CANISTER07/10/2020
7210 mL in 1 CANISTER; Type 0: Not a Combination Product
8NDC:79566-001-08200 in 1 CANISTER07/10/2020
8420 mL in 1 CANISTER; Type 0: Not a Combination Product
9NDC:79566-001-09400 in 1 CONTAINER07/10/2020
9840 mL in 1 CONTAINER; Type 0: Not a Combination Product
10NDC:79566-001-10500 in 1 CONTAINER07/10/2020
101050 mL in 1 CONTAINER; Type 0: Not a Combination Product
11NDC:79566-001-11750 in 1 CONTAINER07/10/2020
111575 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/10/2020
Labeler - Vaxman Group 2015 Ltd. (531964346)

Revised: 7/2020
Document Id: aa1751f5-1d78-2d5f-e053-2a95a90a58f7
Set id: aa17865e-8cf9-7a4e-e053-2a95a90a6f34
Version: 1
Effective Time: 20200710
 
Vaxman Group 2015 Ltd.