VCO UV CLEAR SUNSCREEN

Manufacturer
Shenzhen Heliansheng Trading Co., Ltd.
Effective date
2024-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:10:15

Label at a glance#

ProductVCO UV CLEAR SUNSCREEN
Active ingredientOCTOCRYLENE
Label structure7 sections

Dosage and administration

After Basic Skin Care, Apply Appropriate Amount Of This Product On Face And Neck Skin, Pat Evenly In Forehead, Nose, Cheek And Chin. Any Blemishes On The Face Can Be Reapplied To Cover The Blemishes Better.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

helps prevent sunburn

higher SPF gives more sunburn protection

Warning

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If Swallowed

OTHER SAFETY INFORMATION

Get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

After Basic Skin Care, Apply Appropriate Amount Of This Product On Face And Neck Skin, Pat Evenly In Forehead, Nose, Cheek And Chin. Any Blemishes On The Face Can Be Reapplied To Cover The Blemishes Better.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER、CYCLOPENTASILOXANE、CYCLOHEXASILOXANE、METHYLPROPANEDIOL、ALUMINA、LAUROYL LYSINE、ETHYLHEXYL METHOXYCINNAMATE、BHT、ETHYLHEXYL SALICYLATE、ISONONYL ISONONANOATE、LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE、PHENYLBENZIMIDAZOLE SULFONIC ACID、DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE、DIISOSTEARYL MALATE、CETYL PEG/PPG-10/1 DIMETHICONE、TRIMETHYLSILOXYSILICATE、SODIUM CHLORIDE、POLYETHYLENE、TRIETHOXYCAPRYLYLSILANE、QUATERNIUM-18、BENTONITE、SODIUM HYDROXIDE、PHENOXYETHANOL、ALCOHOL、DIPOTASSIUM GLYCYRRHIZATE、SODIUM HYALURONATE、FRAGRANCE、CI 77891、CI 77492、CI 77491、CI 77499

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

jiu-50gjiu-50g

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84191-001-012025-07-29C16284748780-13b156c62-2a77-fb37-e063-e6dba90a4e0784191-001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84191-001-01VCO UV CLEAR SUNSCREEN50 g in 1 BOTTLEOINTMENT501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84191-001VCO UV CLEAR SUNSCREEN (OCTOCRYLENE) OINTMENT [SHENZHEN HELIANSHENG TRADING CO., LTD.]11 package rows20240327_1488bf27-007c-ee69-e063-6294a90a4023.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84191-00184191-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
1488bf27-007d-ee69-e063-6294a90a40231488bf27-007c-ee69-e063-6294a90a40232024-03-25WarningsExact identifier
spl id: 1488bf27-007d-ee69-e063-6294a90a4023
spl set id: 1488bf27-007c-ee69-e063-6294a90a4023

Reported adverse events (FAERS/openFDA)#

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