DOCTOR HAND FRESS Gel by C-MAX KOREA CO.,LTD. Drug Facts

DOCTOR HAND FRESS Gel by

Drug Labeling and Warnings

DOCTOR HAND FRESS Gel by is a Otc medication manufactured, distributed, or labeled by C-MAX KOREA CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOCTOR HAND FRESS GEL- alcohol gel 
C-MAX KOREA CO.,LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Drug Facts

ethanol

water, carbopol, polysorbate 60, triethanolamine, peppermint oil

Antiseptic

instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

instant hand antiseptic to decrease bacteria on the skin
recommended for repeated use

KEEP OUT OF REACH OF THE CHILDREN

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

for external use only

DOCTOR HAND FRESS GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70949-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	310 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
PEPPERMINT (UNII: V95R5KMY2B)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 60 (UNII: CAL22UVI4M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70949-001-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/02/2020	04/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/21/2020	04/06/2020

Labeler - C-MAX KOREA CO.,LTD. (557821673)

Registrant - C-MAX KOREA CO.,LTD. (557821673)

Establishment
Name	Address	ID/FEI	Business Operations
C-MAX KOREA CO.,LTD.		557821673	manufacture(70949-001)

Revised: 4/2020

Document Id: a2aaca4a-db95-79c8-e053-2a95a90ae72a

34390-5

Set id: a25f52ad-50fe-6b6c-e053-2a95a90a4760

Version: 2

Effective Time: 20200406