CVS HAND SANITIZER- alcohol spray 
CVS

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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Drug Facts

Active ingredient

Ethyl Alcohol 63.00%

Purpose

Antiseptic

Keep Out of Reach of Children

If swallowed get medical help or contact a Poison Control Center right away.

Uses

For handwashing to decrease bacteria on the skin that may cause disease. Recommended for repeat use.

Warnings

For external use only: Hands. Flammable. Keep away from flame.

When using this product: keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor: if irritation develops.

Directions

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Blue 1, Dimethicone, Disodium EDTA, DMDM Hydantoin, Fragrance, Polysorbarte, Propanediol, Tocopherol (Vitamin E), Water, Yellow 5.

Package/Label Principal Display Panel

CVS Instant Hand Sanitizer Spray
CVS HAND SANITIZER 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-557
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL56 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K) 0.010 mg  in 1 g
PROPANEDIOL (UNII: 5965N8W85T) 1.7 mg  in 1 g
POLYSORBATE 20 (UNII: 7T1F30V5YH) 4.46 mg  in 1 g
DIMETHICONE (UNII: 92RU3N3Y1O) .12 mg  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-557-011 g in 1 CONTAINER; Type 0: Not a Combination Product08/17/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/17/2015
Labeler - CVS (062312574)
Registrant - OraLabs (801824756)
Establishment
NameAddressID/FEIBusiness Operations
OraLabs801824756MANUFACTURE(69842-557) , LABEL(69842-557)

Revised: 8/2015
Document Id: d0081c50-c0d2-436a-ba83-5d1982ae64b7
Set id: d0081c50-c0d2-436a-ba83-5d1982ae64b7
Version: 1
Effective Time: 20150817
 
CVS