FDA.reportPublic FDA data

MEDI UV PROTECTION 120

Manufacturer
DERMA CENTRIC INC
Effective date
2020-08-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:19

Label at a glance#

ProductMEDI UV PROTECTION 120
Active ingredientTITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide

OTC - PURPOSE SECTION

UV protection

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

WATER
ZINC OXIDE
CYCLOPENTASILOXANE
ETHYLHEXYL METHOXYCINNAMATE
DIMETHICONE
ETHYLHEXYL SALICYLATE
COCO-CAPRYLATE/CAPRATE
GLYCERIN
BUTYLOCTYL SALICYLATE
LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICON
DIPROPYLENE GLYCOL
CAPRYLYL METHICONE
SILICA
ECHIUM PLANTAGINEUM SEED OIL
PORTULACA OLERACEA EXTRACT
CENTELLA ASIATICA EXTRACT
HOUTTUYNIA CORDATA EXTRACT
CURCUMA LONGA (TURMERIC) ROOT EXTRACT
SALVIA HISPANICA SEED EXTRACT
CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE
DISTEARDIMONIUM HECTORITE
MAGNESIUM SULFATE
METHYL METHACRYLATE CROSSPOLYMER
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER
POLYGLYCERYL-6 POLYRICINOLEATE
PROPANEDIOL
ALUMINUM HYDROXIDE
TRIETHOXYCAPRYLYLSILANE
ALUMINUM STEARATE
CAPRYLYL GLYCOL
OCTYLDODECANOL
CETEARYL DIMETHICONE CROSSPOLYMER
GLYCERYL CAPRYLATE
SACCHARIDE HYDROLYSATE
ETHYLHEXYLGLYCERIN
MICROCRYSTALLINE CELLULOSE
1,2-HEXANEDIOL
CELLULOSE GUM
MADECASSOSIDE
SODIUM HYALURONATE
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES
TOCOPHEROL
FRAGRANCE

INDICATIONS & USAGE SECTION

apply proper amount to the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79593-0003-12022-01-28C16284748780-1d6a99b39-796b-a426-e053-dadaa90af4c2ac6667fe-3f39-6436-e053-2a95a90af74a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79593-0003-1MEDI UV PROTECTION 12050 mL in 1 TUBESHAMPOO501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79593-0003MEDI UV PROTECTION 120 (TITANIUM DIOXIDE) SHAMPOO [DERMA CENTRIC INC]1Legacy NDC, 1 package rows20200811_ac6667fe-3f39-6436-e053-2a95a90af74a.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79593-000379593-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
PROPANEDIOL5965N8W85TIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
DIMETHICONE92RU3N3Y1OIACT

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
ac66685c-9dd3-ccb0-e053-2995a90ace66ac6667fe-3f39-6436-e053-2a95a90af74a2020-08-08WarningsExact identifier
spl id: ac66685c-9dd3-ccb0-e053-2995a90ace66
spl set id: ac6667fe-3f39-6436-e053-2a95a90af74a

Reported adverse events (FAERS/openFDA)#

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