SRRIPO 20% VITAMIN C SERUM- serum liquid

Srripo 20% VITAMIN C SERUM by

Drug Labeling and Warnings

Srripo 20% VITAMIN C SERUM by is a Otc medication manufactured, distributed, or labeled by Guangdong Miaolian Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

After cleansing or afterusing the toner, apply an appropriateamount of the essence to the skin andgently massage until absorbed.

WARNINGS

Forevemaluseony Avoid coniac wth eves li coniac ocus nse ihorouthly wt waier

Keep out ofreach oi chidrenifvou ale preanant.nursing.

Consutyou healthcare provider before using the product

INACTIVE INGREDIENT

BUTYLENE GLYCOL

INDICATIONS & USAGE

Do not place it in the sunor high temperature, please keep it outof reach of infants and young children.

Due to the differences in the skin ofeach person,it is recommended to trythis product behind the ear beforeusing it for the first time.

lf you haveany discomfort,please discontinue.
Avoid placing it in directsunlight, please keep it in a cool place.

KEEP OUT OF REACH OF CHILDREN

Please keep it outof reach of infants and young children.

PURPOSE

Enriched with vitamin C andother antioxidants, this serumbrightens the complexion, reducesthe appearance of dark spots andwrinkles, and leaves your skin radiant.Skin looks hydrated, smooth and firm.

ACTIVE INGREDIENT

20% ASCORBIC ACID

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SRRIPO 20% VITAMIN C SERUM 
serum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84507-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	20 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TOCOPHEROL (UNII: R0ZB2556P8)
EQUUS CABALLUS COLLAGEN (UNII: 3221SCV0LS)

Product Characteristics
Color	orange	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84507-029-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/11/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	02/11/2025

Labeler - Guangdong Miaolian Cosmetics Co., Ltd. (707598469)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Miaolian Cosmetics Co., Ltd.		707598469	label(84507-029) , manufacture(84507-029)