SHINE K CAMELLIA HAND SANITIZER- alcohol gel

SHINE K CAMELLIA HAND SANITIZER by

Drug Labeling and Warnings

SHINE K CAMELLIA HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by MLS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

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 this product

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

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, Butylene Glycol. Carbomer, Triethanolamine

Package Label

INGREDIENTS AND APPEARANCE

SHINE K CAMELLIA HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73984-318
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	36.4 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.3 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	1 mL  in 100 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	0.3 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73984-318-01	2 mL in 1 POUCH; Type 0: Not a Combination Product	04/10/2020
2	NDC: 73984-318-02	30 mL in 1 POUCH; Type 0: Not a Combination Product	04/10/2020
3	NDC: 73984-318-04	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/10/2020
4	NDC: 73984-318-03	80 mL in 1 TUBE; Type 0: Not a Combination Product	04/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/10/2020

Labeler - MLS (689850283)

Registrant - MLS (689850283)

Establishment
Name	Address	ID/FEI	Business Operations
MLS		689850283	manufacture(73984-318)