THE FACT NATURAL SFN 18 SKIN TONER- niacinamide, adenosine liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4), ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)

Available from:

Interkos Co.,Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

for skin protectant Take an appropriate amount on your hands and apply it to your face.

Authorization status:

unapproved drug other

Summary of Product characteristics

THE FACT NATURAL SFN 18 SKIN TONER- NIACINAMIDE, ADENOSINE LIQUID
INTERKOS CO.,LTD.
_Disclaimer: This drug has not been found by FDA to be safe and
effective, and this_
_labeling has not been approved by FDA. For further information about
unapproved_
_drugs, click here._
----------
DRUG FACTS
niacinamide, adenosine
water, carbomer, sorbitol, allantoin, glycerin, etc
for skin protectant
KEEP OUT OF REACH OF THE CHILDREN
Take an appropriate amount on your hands and apply it to your face.
1) Please consult your doctor if you experience side effects such as
swelling, itching, or
reddening on the area where you applied this product
2) Do not apply on wounds or cuts. 3) Do not store where children may
reach, and
avoid keeping it exposed to direct sunlight.
external use only
THE FACT NATURAL SFN 18 SKIN TONER
niacinamide, adenosine liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:77049-0012
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)
NIACINAMIDE
2 g in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)
ADENOSINE
0.04 g in 100 mL
Interkos Co.,Ltd.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:77049-
0012-1
150 mL in 1 BOTTLE; Type 0: Not a Combination
Product
01/21/2022
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved drug
other
01/21/2022
LABELER -
Interkos Co.,Ltd. (689850314)
REGISTRANT -
Interkos Co.,Ltd. (689850314)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Interkos Co.,Ltd.
689850314
manufacture(77049-0012)
Revised: 1/2022