DRP HAND SANITIZER- ethyl alcohol gel 
Europremier, S.A. de C.V.

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.

----------

drp Hand Sanitizer 

DRUG FACTS

Active ingredients

Ethyl alcohol 70%

Purpose

Antiseptic Alcohol

Use For handwashing to decrease bacteria on skin. Only when water is not available.

Warnings For external use only. Flammable. Keep away from flame or high heat.

When using this product Keep out of eyes. In case of contact, rinse eyes with water. Avoid contact with broken skin. Do not ingest or inhale.

Stop use and ask a doctor if Irritation or redness develop.

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

Directions Rub hands thoroughly with product. Allow to dry without whiping, for children under 6, use only with adult supervision.

Other information Do not store above 105°F. May discolor fabrics. Harmful to wood finishes and plastics.

Inactive ingredients Water, glycerin, preservative, carbomer, triethanolamine, fragrance, D&C Violet #2

Green Apple

70% alcohol

Made in Mexico by

Europremier S.A. de C.V.

108 Cerezos St., Santa María

Totoltepec, 50200, Toluca,

Mexico

+52 722 199 4990

Packaging

IMAGE

DRP HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79202-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79202-001-11500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
2NDC:79202-001-221000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
3NDC:79202-001-333785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/01/2020
Labeler - Europremier, S.A. de C.V. (951579107)
Establishment
NameAddressID/FEIBusiness Operations
Europremier, S.A. de C.V.951579107manufacture(79202-001)

Revised: 7/2020
Document Id: 8a48f7d1-2f80-45f4-9fe8-e63b580617ec
Set id: 5e1451aa-3e5e-4430-a58f-d3ac3c426a98
Version: 2
Effective Time: 20200707
 
Europremier, S.A. de C.V.