LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE

Manufacturer
Dermafirm INC. | EYESOME. Co.,Ltd.
Effective date
2019-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:44

Label at a glance#

ProductLABODE DERMAFIRM SUN DEFENSE MAKE UP BASE
Active ingredientZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate(Octinoxate), Ethylhexyl Salicylate(Octisalate), Titanium Dioxide, Zinc Oxide

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Cyclohexasiloxane, Butylene Glycol, Polyglyceryl-4 Isostearate, PEG-10 Dimethicone, Hydrogenated Poly(C6-14 Olefin), Cetyl PEG/PPG-10/1 Dimethicone, Cetyl Ethylhexanoate, Betaine, Cyclomethicone, Magnesium Sulfate, Disteardimonium Hectorite, Methyl Methacrylate Crosspolymer, Aluminum Hydroxide, Stearic Acid, Caprylyl Glycol, Dextrin Palmitate, Dimethicone Crosspolymer, Phenyl Trimethicone, Sodium Guaiazulene Sulfonate, Glycerin, Caprylhydroxamic Acid, Allantoin, Aloe Barbadensis Leaf Juice, Perilla Ocymoides Leaf Extract, Phenoxyethanol, Biosaccharide Gum-4, Citric Acid, Potassium Sorbate, Sodium Benzoate, Fragrance

OTC - PURPOSE SECTION

Helps prevent sunburn.

Helps improve skin tone and keep moisturized.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

After the basic skincare routine, apply a suitable amount and gently spread.

WARNINGS SECTION

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71638-0014-12021-07-23C16284748780-1c7ccaba7-19a4-fd44-e053-dadaa90aa01bDermafirm - LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE (71638-0013)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71638-0014-1LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE30 g in 1 TUBE, WITH APPLICATORCREAM302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71638-0014LABODE DERMAFIRM SUN DEFENSE MAKE UP BASE (ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [DERMAFIRM INC.]2Legacy NDC, 1 package rows20191204_97a9d2ca-e817-e135-e053-2a95a90ae5c1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71638-001471638-0014-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
98d7e5df-e3ad-379b-e053-2995a90a41fa97a9d2ca-e817-e135-e053-2a95a90ae5c12019-12-03WarningsExact identifier
spl id: 98d7e5df-e3ad-379b-e053-2995a90a41fa
spl set id: 97a9d2ca-e817-e135-e053-2a95a90ae5c1

Reported adverse events (FAERS/openFDA)#

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