Post rays Blemish Balm

Manufacturer
Humex,Inc | HANACOS CO., LTD.
Effective date
2020-01-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:46:59

Label at a glance#

ProductPost rays Blemish Balm
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure7 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

▪ Appy 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

Zinc Oxide (3.5%)--------------------------Sunscreen

Titanium Dioxide (5.99%)---------------Sunscreen

Octinoxate (6.5%)-------------------------Sunscreen packaging with label in placepackaging with label in place

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

▪ Appy 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, Cetyl Ethylhexanoate, Propylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Isononyl Isononanoate, Clydomethicones, Sorbitan Sesquioleate, Talc, Mineral Oil, Arbutin, Medium-Chain Triglyceride, Microcrystalline Wax, Magnesium Sulfate, Dimethicone, Bentoquatam, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Phenoxyethanol, Ferric Oxide Yellow, Ferrosoferric Oxide, Ferric Oxide Red, Aluminum Hydroxide, PEG-10 Dimethicone Crosspolymer, Triethoxycaprylylsilane, Allantoin, Adenosine, Purslane, Aloe Vera Leaf, Chamaemelum Nobile Flower, Hyaluronate Sodium

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label in placelabel in place

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
76344-800376344-8003-1, 76344-8003-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
d57ecfcc-e89f-1896-e053-2a95a90ad18a9aa584ce-5541-294f-e053-2a95a90a46352022-01-13WarningsExact identifier
spl set id: 9aa584ce-5541-294f-e053-2a95a90a4635

Reported adverse events (FAERS/openFDA)#

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