PURE VELOCITY MINERAL SUNSCREEN SPF 50- zinc oxide cream

Pure velocity MINERAL SUNSCREEN SPF 50 by

Drug Labeling and Warnings

Pure velocity MINERAL SUNSCREEN SPF 50 by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

ZINC OXIDE

Purpose

SUNSCREEN

Uses

If used as directed with other sun protection measures(see Directions)，
decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only

Stop Use

Rinse with wate to remove.
Stop use and ask doctor if rash occurs.

Do Not Use

Do not use on damaged or broken skin.

When Using

When using this product keep out of eyes.

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

Dosage & administration

Squeeze out an appropriate amount of Sunscreen and spread evenly on skin.

Inactive ingredients

WATER
GLYCEROL
PROPYLENE GLYCOL
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
POLYGLYCERYL-2 TRIISOSTEARATE
PHENYL TRIMETHICONE
DICAPRYLYL CARBONATE
TRIMETHYLSILOXYSILICATE
CERA ALBA
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
BENTONITE
SODIUM CHLORIDE
ASCORBIC ACID POLYPEPTIDE
CERAMIDE NP
SPHINGOMONAS FERMENT EXTRACT
SILICA
MAGNESIUM STEARATE
PEG-30 DIPOLYHYDROXYSTEARATE
XANTHAN GUM
SODIUM HYALURONATE
BISABOLOL
TOCOPHEROL
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
SOLANUM LYCOPERSICUM (Tomato) FRUIT EXTRACT
TREMELLA FUCIFORMIS (Mushroom) EXTRACT
LILIUM CANDIDUM FLOWER EXTRACT
DENDROBIUM NOBILE EXTRACT
STEPHANIA TETRANDRA EXTRACT
TARAXACUM OFFICINALE (Dandelion) LEAF EXTRACT
SAURURUS CHINENSIS LEAF/ROOT EXTRACT
PARFUM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE VELOCITY MINERAL SUNSCREEN SPF 50 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BISABOLOL (UNII: 24WE03BX2T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STEPHANIA TETRANDRA WHOLE (UNII: 7S7TV2F4XC)
TARAXACUM OFFICINALE (DANDELION) ROOT (UNII: 9DE5YCO0RU)
SOLANUM LYCOPERSICUM (TOMATO) FRUIT (UNII: Z4KHF2C175)
PARFUMIDINE (UNII: A2Q2LHC6MA)
MYCOPLASMA FERMENTANS (UNII: 3U6TN9Y2LD)
LILIUM CANDIDUM FLOWER OIL (UNII: 6RQW4206B6)
SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
PROPYLENE GLYCOL DIHEXANOATE (UNII: L37F145LOT)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
ALUMINUM HEXAFLUOROSILICATE (UNII: E7I96VX9N6)
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
TOCOPHEROL (UNII: R0ZB2556P8)
DIISOBUTYLPHENOXYETHANOL (UNII: AUK0O5KW1Y)
DIACYLGLYCEROL OIL (UNII: GN1LK75KSX)
BENTONITE (UNII: A3N5ZCN45C)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DENDROBIUM NOBILE WHOLE (UNII: 1Y5P4E7CC6)
TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CERAMIDE NP (UNII: 4370DF050B)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A)
ABIES ALBA LEAF OIL (UNII: G49QS877DA)
TRIMETHYLSILOXYSILICATE (M/Q 0.66) (UNII: 5041RX63GN)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0033-1	50 g in 1 BOTTLE; Type 0: Not a Combination Product	09/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/30/2025

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0033)