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

United States - English - NLM (National Library of Medicine)

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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
Authorization number:
77049-0010-1

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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.

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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 the cream.

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 T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:770 49 -0 0 10

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

NIACINAMIDE (UNII: 25X51I8 RD4) (NIACINAMIDE - UNII:25X51I8 RD4)

NIACINAMIDE

2 g in 10 0 mL

ADENO SINE (UNII: K72T3FS56 7) (ADENOSINE - UNII:K72T3FS56 7)

ADENOSINE

0 .0 4 g in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

BUTYLENE GLYCO L (UNII: 3XUS8 5K0 RA)

Interkos Co.,Ltd.

GLYCERIN (UNII: PDC6 A3C0 OX)

WATER (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:770 49 -0 0 10 -1 150 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

12/14/20 20

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved drug o ther

12/14/20 20

Labeler -

Interkos Co.,Ltd. (689850314)

Registrant -

Interkos Co.,Ltd. (689850314)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Interko s Co .,Ltd.

6 8 9 8 50 314

ma nufa c ture (770 49 -0 0 10 )

Revised: 12/2020

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