Raw antiseptic HAND SANITIZER wipes

Raw antiseptic HAND SANITIZER WIPES by

Drug Labeling and Warnings

Raw antiseptic HAND SANITIZER WIPES by is a Otc medication manufactured, distributed, or labeled by Raw Office Inc, The. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RAW ANTISEPTIC HAND SANITIZER WIPES- ethyl alcohol cloth 
Raw Office Inc, The

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.

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Raw antiseptic HAND SANITIZER wipes

Drug Facts

Active Ingredient:

Ethyl Alcohol 75% (v/v)

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on skin

Warnings

■ External use, not oral. Keep out of children's reach.

■ Flammable, keep away from fire and flame.

■ Use with caution if allergic to alcohol.

When using this product

Avoid contacting face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask doctor if

■ Irritation or redness occurs.

Keep out of children's reach.

If swallowed, get medical help or contact poison control center right away.

Directions

Wet hands thoroughly with product and allow to dry.

Other Information

■ Store below 43°C (110°F)

■ Keep sealed after use

Inactive IngredientsPurified Water, Glycerol, Aloe Vera

Product Use:

Hold and grasp the barrel with both hands then turn the lid counter-clockwise. Take out the wet towel bag, tear the package parallel from the tear hole, pull towel through the centre hole of the barrel lid. Make sure to close lid between uses.

MADE IN CHINA

Packaging

IMAGE

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RAW ANTISEPTIC HAND SANITIZER WIPES 
ethyl alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 75353-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 75353-001-01100 in 1 PACKET08/11/2020
15.4 mL in 1 PACKAGE; Type 0: Not a Combination Product
2NDC: 75353-001-02500 in 1 PACKET11/02/2020
25.4 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/11/202008/11/2022
Labeler - Raw Office Inc, The (204127000)

Revised: 7/2023
 

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