PROTECT CARE HAND SANITIZER - USA- ethyl alcohol gel

Protect Care Hand Sanitizer - USA by

Drug Labeling and Warnings

Protect Care Hand Sanitizer - USA by is a Otc medication manufactured, distributed, or labeled by Antisépticos de México, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash 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.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

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

Inactive ingredients

Water(aqua), Glycerin, Carbomer, Triethanolamine

Package Label - Principal Display Panel 250 mL

250 ml NDC: 76554-003-01

Package Label - Principal display panel 500mL

500 mL NDC: 76554-030-02

PACKAGE LABEL- Principal Display Panel 1000mL

1000 mL NDC: 76554-030-03

INGREDIENTS AND APPEARANCE

PROTECT CARE HAND SANITIZER - USA 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76554-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)	1 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76554-030-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2020
2	NDC: 76554-030-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2020
3	NDC: 76554-030-03	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/05/2020

Labeler - Antisépticos de México, S.A. de C.V. (951576637)

Registrant - Antisépticos de México, S.A. de C.V. (951576637)

Establishment
Name	Address	ID/FEI	Business Operations
Antisépticos de México, S.A. de C.V.		951576637	manufacture(76554-030)