PUVIDA SNOW BLEACH- niacinamide 15% snow bleach cream

PUVIDA SNOW BLEACH by

Drug Labeling and Warnings

PUVIDA SNOW BLEACH by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

NIACINAMIDE 15%

Purpose

elastic and smooth skin

Use

Used to whiten or lighten skin pigmentation.

Warnings

For external use only. on damaged or broken skin. on individwals aged 12 and under.

Do not use

Do not use Stop and ask a doctor. IF irritation or allergic reactions develop.

When Using

When using this product, avoid contact with eyes confact with eyes. Please test this cream on a small patch of your the inside of the arm if it is your first time using this cream.

Stop Use

Stop use section lf pregnant or breast-feeding. ask a health professional before use.

Ask Doctor

Discontinue use if signs of irritation or rash occur.WHEN USING THIS PRODUCT Please clean your hands before use to ensure the best results from the product.

Keep Oot Of Reach Of Children

Please keep out of reach of children.

Directions

1.Apply the product evenly onto clean skin. 2.Massage until fully absorbed. 3. Use daily for several weeks for best results.

Inactive ingredients

WATER , ASCORBIC ACID ，CENTELLA ASIATICA ，CHAMOMILE ，ALLANTOIN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PUVIDA SNOW BLEACH 
niacinamide 15% snow bleach cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-093
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
CHAMOMILE (UNII: FGL3685T2X)
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-093-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	02/08/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)