BABYLISS PRO PROTECT HAND SANITIZER- alcohol gel 
Conair Corporation

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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BABYLISS PRO PROTECT HAND SANITIZER

Drug Facts

Active Ingredient

Ethyl Alcohol 70% V/V

Purpose

Antiseptic

Use

Antibacterial hand sanitizing gel to help kill bacteria and germs as antiseptic on the skin. For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product

keep out of eyes and mouth. In case of contact with eyes, immediately rinse eyes thoroughly with water.

Stop use and ask doctor if

irritation, rash or allergy occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

Apply. Put enough product on hands to cover all surfaces. Rub hands together, until hands feel dry. This should take around 20 seconds. Recommended for repeated use. Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 59-86°F (15-30°C)
Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

Deionized Water. Carbomer. Panthenol. DMDM Hydantoin. Disodium EDTA. Triethanolamine.

Package Labeling

Bottle

BABYLISS PRO PROTECT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12829-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PANTHENOL (UNII: WV9CM0O67Z)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12829-0002-012 in 1 BOX09/25/2020
1488 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/25/2020
Labeler - Conair Corporation (001661222)

Revised: 10/2020
Document Id: b244eb87-9297-9d40-e053-2995a90a5ae6
Set id: b2450142-e2c6-1abb-e053-2a95a90af172
Version: 1
Effective Time: 20201022
 
Conair Corporation