DRUGGIST SUPER C- super c cream

DRUGGIST SUPER C by

Drug Labeling and Warnings

DRUGGIST SUPER C by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Arbutin7% Reduce dark spots
Niacinamide7% Reduce dark spots
4-Butylresorcinol7% Reduce dark spots
Kojic Acid7% Reduce dark spots
Retinol5% Reduce dark spots
Ascorbic Acid5% Anti-oxidation
Glycolic Acid5% Moisturizing

Purpose

Lighten skin spots

Uses

Lighten skin spots, even skin tone, and make skin brighter.

Warnings

For external use only
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs
Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

Do not use

Do not use on damaged or broken skin

When using this product

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

Ask Doctor

When Pregnant or breast-feeding.

Directions

1. After cleansing the face, take an appropriate amount of spot lightening cream.
2. Apply evenly to the area on the face that needs to lighten spots, and massage gently until completely absorbed.
3. Use once in the morning and evening. Continuous use will provide better results.

Other information

Please store in a cool, dry place away from direct sunlight.

Inactive ingredients

Aqua,Methylpropanediol,Butylene Glycol Stearate, Caprylic/Capric /Stearic Triglyceride,Tocopherol,Saccharomyces Polypeptides, BHT,Methylparaben, Propylparaben,Sodium Hyaluronate,Sodium Polyacrylate Starch,Trideceth-6,C18-21 Alkane.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DRUGGIST SUPER C 
super c cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83872-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52)	KOJIC ACID	70 mg  in 1 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	70 mg  in 1 g
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF)	ARBUTIN	70 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
C18-C21 ALKANE (UNII: 33822S0M40)
TRIDECETH-6 (UNII: 3T5PCR2H0C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83872-213-03	50 g in 1 BOTTLE; Type 0: Not a Combination Product	03/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/06/2024

Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xiaomai Manufacturing Co., Ltd.		712999147	manufacture(83872-213)