TALS ACNIC SOOTHING SERUM- salicylic acid liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

salicylic acid

INACTIVE INGREDIENT

Camellia Sinensis Leaf Water
Propanediol
Pentylene Glycol
Allium Cepa (Onion) Bulb Extract
Lycium Chinense Fruit Extract
Niacinamide
Glycerin
Glycyrrhiza Glabra (Licorice) Root Extract
Ammonium Acryloyldimethyltaurate/VP Copolymer
Panthenol
Centella Asiatica Extract
Prunella Vulgaris Flower/Leaf/Stem Extract
Hydrolyzed Rice Bran Extract
Salix Alba (Willow) Leaf Extract
Water(Aqua)
Xanthan Gum
Citrus Unshiu Peel Extract
Caprylyl Glycol
Salicylic Acid
Hyaluronic Acid
Soy Isoflavones
Spinacia Oleracea (Spinach) Leaf Extract
Citrus Junos Fruit Extract
Pinus Densiflora Leaf Extract
Sorbitan Caprylate
Artemisia Annua Extract
Levulinic Acid
Magnolia Liliflora Bud Extract
Aniba Rosodora (Rosewood) Wood Oil
Geranium Maculatum Oil
Santalum Album (Sandalwood) Oil
Rose Flower Oil

PURPOSE

visibly reduces the appearance of acne & blemishes

controls sebum production and tightens the pores

suitabgle for oily & acne-prone skin

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

After cleanisng, apply iberal amount onto entire face. Pay particular attention to the troubled area.

WARNINGS

for external use only

do not use if sensitive to any of the ingredients

discontinue use if signs of irritation or rash appear

if irritation or rash persists, contact a doctor

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TALS ACNIC SOOTHING SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72289-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PANTHENOL (UNII: WV9CM0O67Z)
NIACINAMIDE (UNII: 25X51I8RD4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72289-0002-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/24/2019

Labeler - SKINCURE INC (557830240)

Registrant - SKINCURE INC (557830240)

Establishment
Name	Address	ID/FEI	Business Operations
SKINCURE INC		557830240	label(72289-0002) , manufacture(72289-0002)