FDA.reportPublic FDA data

Facial moisturizing sunscreen

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-10-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:23:13

Label at a glance#

ProductFacial moisturizing sunscreen
Active ingredientEQUINE COLLAGEN
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrolyzed Collagen

Inactive ingredient

INACTIVE INGREDIENT SECTION

Aqua, glycerin, titanium dioxide,Tocopherol, DL-Alpha.

Purpose section

OTC - PURPOSE SECTION

Can absorbor reflect ultraviolet rays,Effectively protects skinfrom damage under thesun in outdoor activitycenters.

Warning

WARNINGS SECTION

Sensitivity testing for newusers. Apply productsparingly to one or twosmall affected areas forthe first 3 days. lf nodiscomfort occurs. Pleasefollow the instructionsabove.

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

As the final step inyour skin care routine, usebefore makeup. lt ishighly recommended toapply sunscreen at least30 minutes before startingoutdoor activities formaximum effectiveness.

Dosage

DOSAGE & ADMINISTRATION SECTION

It is recommended to use enough sunscreen to cover the entire surface of skin exposed to the sun and reapply every 2 hours after each use, especially after swimming, sweating or wiping the skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-032-012025-07-29C16284748780-13b156c62-2828-fb37-e063-e6dba90a4e0723f359c9-a182-ce45-e063-6394a90a4e38

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-032-01Facial moisturizing sunscreen50 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-032FACIAL MOISTURIZING SUNSCREEN CREAM [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241010_23f359c9-a182-ce45-e063-6394a90a4e38.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-03284732-032-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
GLYCERINPDC6A3C0OXIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
EQUINE COLLAGEN3221SCV0LSACTIB

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
23f359c9-a183-ce45-e063-6394a90a4e3823f359c9-a182-ce45-e063-6394a90a4e382024-10-08WarningsExact identifier
spl id: 23f359c9-a183-ce45-e063-6394a90a4e38
spl set id: 23f359c9-a182-ce45-e063-6394a90a4e38

Reported adverse events (FAERS/openFDA)#

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