Pop Zinc Sunscreen

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd | Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:51:09

Label at a glance#

ProductPop Zinc Sunscreen
Active ingredientZINC OXIDE
Label structure11 sections

Indications and 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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Non-Nano Zinc Oxide 5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Dosage

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

INDICATIONS & USAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0009-1Pop Zinc Sunscreen100 mL in 1 BOTTLESPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60771-0009POP ZINC SUNSCREEN (ZINC OXIDE) SPRAY [GUANGZHOU HAISHI BIOLOGICAL TECHNOLOGY CO., LTD]1Current NDC, 1 package rows20250109_2b29ddb2-5730-8a67-e063-6394a90ae416.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-000960771-0009-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pop Zinc SunscreenZINC OXIDEGuangzhou Haishi Biological Technology Co., Ltd2b29ddb2-5730-8a67-e063-6394a90ae4162025-01-07WarningsExact identifier
ndc (package): 60771-0009-1
ndc (product): 60771-0009
ndc11 (package): 60771000901
spl id: 2b29ddb2-5731-8a67-e063-6394a90ae416
spl set id: 2b29ddb2-5730-8a67-e063-6394a90ae416

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.