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 Hemei 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

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.

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: 84010-051
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
ALLANTOIN (UNII: 344S277G0Z)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
WATER (UNII: 059QF0KO0R)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CHAMOMILE (UNII: FGL3685T2X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-051-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/27/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-051)