POP ZINC SUNSCREEN- zinc oxide spray

Pop Zinc Sunscreen by

Drug Labeling and Warnings

Pop Zinc Sunscreen by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd, Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Non-Nano Zinc Oxide 5%

Purpose

Sunscreen

Warnings

For external use only.

Stop use and ask a doctor if

rash occurs.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Dosage

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

Inactive ingredients

Inactive ingredients

AQUA (WATER) 67.6%
GLYCERIN 5%
SHEA BUTTER ETHYL ESTERS 5%
OLIVE OIL GLYCERETH-8 ESTERS 6%
ORYZA SATIVA (RICE) EXTRACT 0.8%
ALOE BARBADENSIS (ALOE VERA) LEAF EXTRACT 0.8%
APHANIZOMENON FLOSAQUAE (BLUE GREEN ALGAE) EXTRACT 0.8%
CUCURBITA PEPO (PUMPKIN) SEED EXTRACT 1%
PUNICA GRANATUM (POMEGRANATE) EXTRACT 1%
VACCINIUM ANGUSTIFOLIUM (BLUEBERRY) FRUIT EXTRACT 0.5%
MALPIGHIA GLABRA (ACEROLA) FRUIT EXTRACT 0.5%
STEPHANIA TETRANDRA EXTRACT 0.5%
TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT 0.5%
SAURURUS CHINENSIS LEAF/ROOT EXTRACT 0.5%
XYLITOL CAPRYLATE/​CAPRATE 1%
TRIETHOXYCAPRYLYLSILANE 1.5%
GLUCONO DELTA LACTONE 1%
TOCOPHEROL 1%

Uses

Shake well before use.
Hold the spray in hand and apply it 15-20cm from the skin.
Apply liberally 15 minutes before sun
exposure and reapply every 2 hoursthroughout the day

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POP ZINC SUNSCREEN 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0009
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
TOCOPHEROL (UNII: R0ZB2556P8)
MALPIGHIA GLABRA (ACEROLA) FRUIT (UNII: B94O42LA9M)
OLIVE OIL GLYCERETH-8 ESTERS (UNII: 322K2STO13)
SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)
APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0009-1	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/08/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/08/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0009)