EMELY HAND SANITIZER- alcohol gel

Emely Hand Sanitizer by

Drug Labeling and Warnings

Emely Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Laboratorios E&M SRL. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 80% v/v Purpose: Antiseptic

Purpose

Aseptic, Hand Sanitizer

Uses

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

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

Glicerin, Purified Water USP, Triethanolamine, Carbomer

Package Label - Principal Display Panel

​60 mL NDC: 77998-001-10

Package Label - Principal Display Panel

120 mL NDC: 77998-001-20

Package Label - Principal Display Panel

240 mL NDC: 77998-001-30

Package Label - Principal Display Panel

480 mL NDC: 77998-001-40

Package Label - Principal Display Panel

960 mL NDC: 77998-001-50

Package Label - Principal Display Panel

1920 mL NDC: 77998-001-60

Package Label - Principal Display Panel

3785 mL NDC: 77998-001-70

INGREDIENTS AND APPEARANCE

EMELY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77998-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77998-001-10	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
2	NDC: 77998-001-20	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
3	NDC: 77998-001-30	240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
4	NDC: 77998-001-40	480 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
5	NDC: 77998-001-50	960 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
6	NDC: 77998-001-60	1920 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
7	NDC: 77998-001-70	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Laboratorios E&M SRL (817468959)

Establishment
Name	Address	ID/FEI	Business Operations
Laboratorios E&M SRL		817468959	manufacture(77998-001) , analysis(77998-001) , pack(77998-001) , label(77998-001)