SANISMART 3- ethanol liquid 
Registered Chemicals 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.

----------

Active ingredient

Ethanol 70%

Purpose

Antimicrobial

Uses    •For hand washing to decrease bacteria on the skin

            •Recommended for repeated use

Warnings

For external use only.

Flammable, keep away from fire or flame.

When using this product avoid contact with eyes. In case of eye contact, flush eyes

thoroughly with water.

Stop use and ask a doctor if irritation or redness develop, or if condition persists for more

than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a

Poison Control Center right away.

Directions    •Dispense an adeqaute amount in your palm to cover all surfaces of hands

completely.    •Rub hands together until dry   •Supervise children in the use of this product.

Other information   •Do not store above 100° F (38° C)   •May discolor some fabrics

Inactive ingredients   Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Barbadensis Leaf

Juice Panthenol

Questions or comments?   781-03-7800   •info@registeredchemicals.com

image description

image description

SANISMART 3 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72130-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PANTHENOL (UNII: WV9CM0O67Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72130-003-011250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2018
2NDC:72130-003-021000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2018
3NDC:72130-003-033750 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2018
Labeler - Registered Chemicals Corporation (046652831)

Revised: 3/2018
Document Id: 4ebfd119-ec0a-4e11-ac1d-5384e831f211
Set id: ecfa5e4a-ed70-4f32-87ea-0e60c8dac3d0
Version: 2
Effective Time: 20180314
 
Registered Chemicals Corporation