CLEACE- ethyl alcohol gel

CLEACE by

Drug Labeling and Warnings

CLEACE by is a Otc medication manufactured, distributed, or labeled by Nanjing Aogrand Int'l Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol

Purpose

Antiseptic

Uses

• hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
• recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

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

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children must be supervised in use of this product.

Directions

• place enough product into your palms and thoroughly spread on both hands.
• rub into skin until dry.

Other information

• store below 110°F (43°C).
• may discolor certain fabrics or surfaces.

Inactive ingredients

carbomer, triethanolamine, glycerin, water

1oz CLEACE

2oz CLEACE

3.4oz CLEACE

8oz CLEACE

10oz CLEACE

16.9oz CLEACE

33.8oz CLEACE

39.9oz CLEACE

50.7 oz CLEACE

169.1oz CLEACE

676.3oz CLEACE

INGREDIENTS AND APPEARANCE

CLEACE 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74621-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	7.5 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74621-002-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
2	NDC: 74621-002-02	60 mL in 1 PACKAGE; Type 0: Not a Combination Product	04/07/2020
3	NDC: 74621-002-03	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
4	NDC: 74621-002-04	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
5	NDC: 74621-002-05	296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
6	NDC: 74621-002-06	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
7	NDC: 74621-002-07	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
8	NDC: 74621-002-08	1180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
9	NDC: 74621-002-09	1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
10	NDC: 74621-002-10	5000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020
11	NDC: 74621-002-11	20000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2020

Labeler - Nanjing Aogrand Int'l Corp (421353092)

Establishment
Name	Address	ID/FEI	Business Operations
Nanjing Aogrand Int'l Corp		421353092	manufacture(74621-002)