Post Rays UV Protect Sun Block

Manufacturer
Humex,Inc | Kolmar Korea
Effective date
2021-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:49

Label at a glance#

ProductPost Rays UV Protect Sun Block
Active ingredientOCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

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

Label contents#

Full prescribing information#

Drug Facts Active Ingredient Purpose

OTC - ACTIVE INGREDIENT SECTION

packaging with label in placepackaging with label in placeZinc Oxide (5.006%)-----------------------------Sunscreen
Octinoxate (6.8%)--------------------------------Sunscreen
Octisalate (4%)------------------------------------Sunscreen
Titanium Dioxide (4.0014%)-------------------Sunscreen

Uses

OTC - PURPOSE SECTION

Helps prevent sunburn

Warnings

WARNINGS AND PRECAUTIONS SECTION

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

INSTRUCTIONS FOR USE SECTION

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

Other Information

OTHER SAFETY INFORMATION

▪ protect the product in this container from excessive heat and direct sun

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, cyclomethicone, methicone, aluminum hydroxide,dimethicone, dipropylene glycol, peg-10 dimethicone, glycerin, dicaprylyl carbonate, propanediol, saccharide hydrolysate(invert sugar), 1,2-hexandediol, salvia hispanica seed (chia seed) extract, curcuma longa (turmeric) root extract, caprylyl trisiloxane, disteardimonium hectorite, magnesium sulfate, dimethicone/vinyl dimethicone crosspolymer, caprylyl glycol, ethylhexylglycerin, glyceryl monocaprylate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

a representative sample image of a carton/container labela representative sample image of a carton/container label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76344-8002-22023-01-30C16284748780-1f386c64a-3a10-0266-e053-dadaa90a7c1a98fcaac8-b6bc-6e97-e053-2a95a90a7e47

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76344-8002-1Post Rays UV Protect Sun Block50 g in 1 TUBECREAM502
76344-8002-2Post Rays UV Protect Sun Block1 in 1 BOXCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76344-8002POST RAYS UV PROTECT SUN BLOCK (ZINC OXIDE,OCTINOXATE, OCTISALATE,TITAMIUM DIOXIDE) CREAM [HUMEX,INC]2Legacy NDC, 2 package rows20210113_98fcaac8-b6bc-6e97-e053-2a95a90a7e47.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76344-800276344-8002-1, 76344-8002-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML · Source PDF

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
b8a385a9-4bc7-ddac-e053-2995a90afae398fcaac8-b6bc-6e97-e053-2a95a90a7e472021-01-11WarningsExact identifier
spl id: b8a385a9-4bc7-ddac-e053-2995a90afae3
spl set id: 98fcaac8-b6bc-6e97-e053-2a95a90a7e47

Reported adverse events (FAERS/openFDA)#

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