HEMIRUS HAND CLINIC GEL 70%- alcohol gel

Hemirus Hand Clinic Gel 70% by

Drug Labeling and Warnings

Hemirus Hand Clinic Gel 70% by is a Otc medication manufactured, distributed, or labeled by GC US CORPORATION, WOOSIN COSMETICS CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Alcohol 70%

Antiseptic

Uses

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

Warnings

Flammable. Keep away from fire or flame

For external use only.

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

• pump as needed into your palms and throughly spread on both hands.
• rub into skin until dry.

Other Information

• Store at 20 o C (68 o to 77 o F).
• may discolor fabrics.

Inactive Ingredients

Water, Phenoxyethanol, Trolamine, Carbomer homopolymer type C (Allyl pentaerythritol crosslinked)
Methylparaben, Orange, Isopropyl myristate, D&C Orange No. 4, Denatonium benzoate

Questions?

• side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

ACCESSORIES

Instant Hand Sanitizer!

Kills 99.9% of Most Common Germs!

Net Wt. 16.91 fl oz. (500ml)

Manufactured by Woosincosmetics Inc.

33, Sudo-ro, 125beon-gil, Bucheon-si,
Gyeonggi-do, Korea 14491

PRINCIPAL DISPLAY PANEL

500mL NDC: 71454-3041-1

100mL NDC: 71454-3041-2

30mL NDC: 71454-3041-3

INGREDIENTS AND APPEARANCE

HEMIRUS HAND CLINIC GEL 70% 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71454-3041
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
METHYLPARABEN (UNII: A2I8C7HI9T)
ORANGE (UNII: 5EVU04N5QU)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71454-3041-1	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/31/2020
2	NDC: 71454-3041-2	100 mL in 1 TUBE; Type 0: Not a Combination Product	03/31/2020
3	NDC: 71454-3041-3	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/31/2020

Labeler - GC US CORPORATION (080669481)

Establishment
Name	Address	ID/FEI	Business Operations
WOOSIN COSMETICS CO.,LTD		688227829	manufacture(71454-3041)