CLIP HAND SANITIZER- 60% alcohol sanitizer gel 
Shalom, S.A.

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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CLIP Hand Sanitizer

Active ingredient
Ethyl alcohol 60% v/v

354 ml rear label

Purpose

Antiseptic

Uses

To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

Flammable. Keep away from source of heat, fire or flame. For external use only.

When using this product

Avoid contact with eyes. I contact occurs, rinse thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor if

Irritation or redness develops and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Place enough product in your palm to throroughly cover your hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

Inactive ingredients

Water, carbomer, glycerine, triethanolamine, cucumis sativus extract, camellia sinensis (green tea) infusion.

Other information

Store at a temperature below 110ºF (43ºC). May discolor some fabric.

CLIP Hand Sanitizer

354 ml NDC: 78910-001-01

Advanced. Kills up to 99% of bacteria, germs, and other microorganisms. Refreshing gel with cucumber extract and green tea infusion.

354 ml label

CLIP HAND SANITIZER 
60% alcohol sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78910-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
CUCUMBER JUICE (UNII: 61845009SP)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
TEA LEAF OIL (UNII: VC855RRT77)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78910-001-01354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/10/202009/28/2022
Labeler - Shalom, S.A. (846098333)
Registrant - Shalom, S.A. (846098333)
Establishment
NameAddressID/FEIBusiness Operations
Shalom, S.A.846098333manufacture(78910-001)

Revised: 9/2022
 
Shalom, S.A.