JAYSUING SNOW BLEACH CREAM- allantoin cream

JAYSUING Snow Bleach Cream by

Drug Labeling and Warnings

JAYSUING Snow Bleach Cream by is a Otc medication manufactured, distributed, or labeled by Guangdong Ximonth Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

GLUTATHIONE, CENTELLA ASIATICA EXTRACT,ASCORBIC ACID,NIACINAMIDE, CHAMOMILLA RECUTITA(MATRICARIA) FLOWER EXTRACT

Purpose

Elastic and smooth skin

Use

1. Clean and dry skin
2. Apply to skin until completely absorbed
3. For best results, use twice aday in the morning and evening

Warnings

Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place

Do not use

Discontinue use if signs of irritation or rash occur

STOP USE

Discontinue use if signs of irritation or rash occur

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING

Avoid freezing and excessive heat above 40C (104F) ）
Store in a cool and dry place.

INACTIVE INGREDIENT

ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

JAYSUING SNOW BLEACH CREAM 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) (CENTELLA ASIATICA TRITERPENOIDS - UNII:4YS74Q4G4J)	CENTELLA ASIATICA TRITERPENOIDS	6 mg  in 30 mg
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	4.5 mg  in 30 mg
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	4.5 mg  in 30 mg
GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O)	GLUTATHIONE	3 mg  in 30 mg
CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X)	CHAMOMILE	3 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	9 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-024-01	30 mg in 1 BOX; Type 0: Not a Combination Product	09/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/24/2024

Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)

Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ximonth Technology Co., Ltd.		699436264	manufacture(84660-024)