SANDAWHA VITAMIN C BRIGHTENING ESSENCE- ascorbyl glucoside liquid

Sandawha Vitamin C Brightening Essence by

Drug Labeling and Warnings

Sandawha Vitamin C Brightening Essence by is a Otc medication manufactured, distributed, or labeled by SKINCURE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ascorbyl Glucoside

INACTIVE INGREDIENT

Water (Aqua)
Pentylene Glycol
Glycerin
Arginine
Propanediol
Betaine
Niacinamide
Panthenol
Cellulose Gum
Hyaluronic Acid
Polyglyceryl-10 Myristate
Polyglyceryl-10 Laurate
Sorbitan Caprylate
Hordeum Vulgare Seed Extract
Carthamus Tinctorius (Safflower) Seed Oil
Levulinic Acid
Bisabolol
Glycyrrhiza Glabra (Licorice) Root Extract
Naringin
Rutin
Hesperidin
Centella Asiatica Extract
Polygonum Cuspidatum Root Extract
Tocopherol
Camellia Sinensis Leaf Extract
Scutellaria Baicalensis Root Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
Chamomilla Recutita (Matricaria) Leaf Extract
Jasminum Sambac (Jasmine) Flower Extract
Rose Flower Oil

PURPOSE

remove the appearance of dark spots and prevent unwanted skin pigmentation

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply liberal amount on your face. For the best results use twice daily in the morning and the evening.

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

SANDAWHA VITAMIN C BRIGHTENING ESSENCE 
ascorbyl glucoside liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72289-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) (ASCORBYL GLUCOSIDE - UNII:2V52R0NHXW)	ASCORBYL GLUCOSIDE	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: 72289-0013-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/23/2020

Labeler - SKINCURE INC (557830240)

Registrant - SKINCURE INC (557830240)

Establishment
Name	Address	ID/FEI	Business Operations
SKINCURE INC		557830240	label(72289-0013) , manufacture(72289-0013)