SUNSCREEN MOISTURIZER

Manufacturer: Guangzhou Yanxi Biotechnology Co., Ltd
Effective date: 2024-05-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:12:59

Label at a glance#

ProductSUNSCREEN MOISTURIZER

Active ingredientZINC OXIDE, SQUALANE

Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

use as a normal sunscreen

WARNINGS SECTION

For external use only.

INACTIVE INGREDIENT SECTION

AQUA

OTC - PURPOSE SECTION

helps prevent sunburn

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sun exposure. Reapply: After 80 minutes of swimming or sweating, Immediately after towel drying, At least every 2 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84025-038

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84025-038-01	SUNSCREEN MOISTURIZER	150 mL in 1 BOTTLE	CREAM	150		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84025-038	SUNSCREEN MOISTURIZER CREAM [GUANGZHOU YANXI BIOTECHNOLOGY CO., LTD]	1	1 package rows	20240528_19402859-2553-b06e-e063-6294a90ae4a0.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

SUNSCREEN MOISTURIZER
WATER
ZINC OXIDE
SQUALANE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84025-038	84025-038-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ZINC OXIDE	SOI2LOH54Z	ACTIB
SQUALANE	GW89575KF9	ACTIB

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
19402859-2554-b06e-e063-6294a90ae4a0			19402859-2553-b06e-e063-6294a90ae4a0	2024-05-24	Warnings	Exact identifier spl id: 19402859-2554-b06e-e063-6294a90ae4a0 spl set id: 19402859-2553-b06e-e063-6294a90ae4a0

Reported adverse events (FAERS/openFDA)#

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