sunscreen powder

Manufacturer: Guangzhou Fantesy Biotechnology Co.,Ltd
Effective date: 2026-01-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:31:23

Label at a glance#

Productsunscreen powder

Active ingredientZINC OXIDE

Label structure12 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

Apply liberally to face at least 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months of age: Ask a doctor

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 25%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.
Stop use and ask a doctor if rash occurs.
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 immediately.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

When using this product, keep out of eyes. Rinse with water to remove.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

Keep out of

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to face at least 15 minutes before sun exposure.
Use a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
Children under 6 months of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sericite, Mica, and Silica.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83447-001-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83447-001-01	sunscreen powder	3.5 g in 1 BOX	POWDER	3.5		3

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

sunscreen powder
ZINC OXIDE
SILICON DIOXIDE
MICA
PYROPHYLLITE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83447-001	83447-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ZINC OXIDE	SOI2LOH54Z	ACTIB
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
MICA	V8A1AW0880	IACT
PYROPHYLLITE	1U9X05245H	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
sunscreen powder	SUNSCREEN POWDER	Guangzhou Fantesy Biotechnology Co.,Ltd	fae8ecaf-7a9c-902b-e053-6394a90a5f31	2026-01-05	Warnings	Exact identifier ndc (package): 83447-001-01 ndc (product): 83447-001 ndc11 (package): 83447000101 spl id: 479edb42-9157-566b-e063-6394a90a9101 spl set id: fae8ecaf-7a9c-902b-e053-6394a90a5f31

Reported adverse events (FAERS/openFDA)#

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