CLEARSOOTHINGCREAM- hyaluronic acid cream

ClearSoothingCream by

Drug Labeling and Warnings

ClearSoothingCream by is a Otc medication manufactured, distributed, or labeled by Shengnan (Guangzhou) Cosmetics Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS

Please keep out of reach of children.

PURPOSE

Deep hydration locks in moisture and keeps the skin hydrated. Enhances skin elasticity, leaving it smoother and morerefined.

STOP USE

lf irritation occurs.discontinue use and consult a doctor

ACTIVE INGREDIENT

Retinyl Palmitate

WHEN USING

Please keep your skin dry before use to ensure the best results fromthe product.

INACTIVE INGREDIENT

Water
Glycerin
Hyaluronic Acid
Ethylhexyl Palmitate
Polysorbate 60
1,2-Hexanediol
Panthenol
Glyceryl Stearate
Sorbitan Stearate
Carbomer
Collagen
Dipotassium Glycyrrhizate
Disodium EDTA
Tocopheryl Acetate

DOSAGE & ADMINISTRATION

Apply 1-2 times a day

INDICATIONS & USAGE

Take an appropriate amount of theproduct and gently dab it onto the forehead.cheeks, nose, and chin using your fingertips.Gently spread the moisturizer evenly overyour entire face with your fingertips

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLEARSOOTHINGCREAM 
hyaluronic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84019-023
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONIC ACID	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
WATER (UNII: 059QF0KO0R)
PANTHENOL (UNII: WV9CM0O67Z)
POLYSORBATE 60 (UNII: CAL22UVI4M)
SORBITAN STEARATE (UNII: NVZ4I0H58X)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CARBOMER (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84019-023-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/03/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/03/2025

Labeler - Shengnan (Guangzhou) Cosmetics Co., LTD (541200425)

Establishment
Name	Address	ID/FEI	Business Operations
Shengnan (Guangzhou) Cosmetics Co., LTD		541200425	manufacture(84019-023)