FDA.reportPublic FDA data

LUMIOR

Manufacturer
AHAVA Dead Sea Laboratories Ltd
Effective date
2025-07-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:35:06

Label at a glance#

ProductLUMIOR Daylight Moisturizer Broad Spectrum SPF 20
Active ingredientAvobenzone, Homosalate, Octisalate, Octocrylene
Label structure8 sections

Indications and uses

helps prevent sunburn

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Avobenzone [3.0%]sunscreens
Homosalate [7.0%]sunscreens
Octisalate [5.0%]sunscreens
Octocrylene [2.7%]sunscreens

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA (MINERAL SPRING WATER), BUTYLOCTYL SALICYLATE, DIMETHICONE, GLYCERIN, OCTYLDODECYL NEOPENTANOATE, NIACINAMIDE, ASCORBYL GLUCOSIDE (VITAMIN C DERIVATIVE), STYRENE/ACRYLATES COPOLYMER, C12-15 ALKYL BENZOATE, STEARYL ALCOHOL, PEG-100 STEARATE, GLYCERYL STEARATE, SODIUM CITRATE, POTASSIUM CETYL PHOSPHATE, HYDROGENATED OLIVE OIL CETYL ESTERS, PHENOXYETHANOL, HYDROGENATED PALM GLYCERIDES, AMINOMETHYL PROPANOL, CETEARYL ALCOHOL, BENZOTRIAZOLYL DODECYL P-CRESOL, SALICYLIC ACID, TOCOPHERYL (VITAMIN E) ACETATE, PARFUM (FRAGRANCE), XANTHAN GUM, ETHYLHEXYLGLYCERIN, HYDROGENATED POLYDECENE, DIISOBUTYL ADIPATE, BUTYLENE GLYCOL, CITRIC ACID, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, GLYCINE SOJA (SOYBEAN) OIL, HYDROGENATED VEGETABLE GLYCERIDES CITRATE, BETA-SITOSTEROL, ASCORBYL PALMITATE, PROPYLENE GLYCOL, LECITHIN, SODIUM BENZOATE, POTASSIUM SORBATE, SODIUM HYDROXIDE, LACTIC ACID, COMMIPHORA ABYSSINICA RESIN EXTRACT, OPUNTIA FICUS-INDICA FRUIT EXTRACT, SQUALENE (PHYTOSQUALENE), PORPHYRA UMBILICALIS EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SPROUT EXTRACT, ZIZYPHUS JUJUBA FRUIT EXTRACT, PSEUDOALTEROMONAS FERMENT EXTRACT, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, TOCOPHEROL (VITAMIN E), ASCORBIC ACID, RUMEX OCCIDENTALIS EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, ALOE BARBADENSIS LEAF JUICE, PHOENIX DACTYLIFERA (DATE) FRUIT EXTRACT, DUNALIELLA SALINA (DEAD SEA ALGA) EXTRACT, MARIS AQUA (DEAD SEA MINERAL ELIXIR).

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn

Warnings

WARNINGS SECTION

For External Use Only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and consult a doctor if rash or irritation develops and lasts

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical attention or contact a Poison Control Centre right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply every morning in gentle, upward strokes to a clean face and neck. Feel luminous, every day
  • apply daily for a clearer, brighter complexion
  • children under 6 months of age: Ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

  • limit time in the sun, especially from 10a.m.-2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses

Other information

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun

Questions or comments

OTC - QUESTIONS SECTION

Call toll free 1-800-366-7254

SPL UNCLASSIFIED SECTION

Manufactured by AHAVA Dead Sea Laboratories, Dead Sea, Israel, 8698000
In US: AHAVA N.A. LLC, New York, NY 10001

PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LUMIOR
BY AHAVA

LUMINOUS

DAYLIGHT MOISTURIZER
BROAD SPECTRUM SPF 20

HYDRATANT DAYLIGHT
PROTECTION SPF 20

PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton
PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60289-297-242023-11-15C16284748780-1f386c649-adc3-0266-e053-dadaa90a7c1aLUMIOR Daylight Moisturizer Broad Spectrum SPF 20
60289-297-242023-01-30C16284748780-1f386c649-adc3-0266-e053-dadaa90a7c1aLUMIOR Daylight Moisturizer Broad Spectrum SPF 20

Products#

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

DailyMed product names page 1 of 2 · 53 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60289-29760289-297-24

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 51 matching rows.

Name, UNII, Kind table
NameUNIIKind
AvobenzoneG63QQF2NOXACTIB
HomosalateV06SV4M95SACTIB
Octisalate4X49Y0596WACTIB
Octocrylene5A68WGF6WMACTIB
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERINPDC6A3C0OXIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
NIACINAMIDE25X51I8RD4IACT
ASCORBYL GLUCOSIDE2V52R0NHXWIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PEG-100 STEARATEYD01N1999RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
HYDROGENATED OLIVE OIL CETYL ESTERSAUR5S128JMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
HYDROGENATED PALM GLYCERIDESYCZ8EM144QIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
BENZOTRIAZOLYL DODECYL P-CRESOL298PX4M11XIACT
SALICYLIC ACIDO414PZ4LPZIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
XANTHAN GUMTTV12P4NEEIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIISOBUTYL ADIPATE8OPY05ZY7SIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
SOYBEAN OIL241ATL177AIACT
.BETA.-SITOSTEROLS347WMO6M4IACT
ASCORBYL PALMITATEQN83US2B0NIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM HYDROXIDE55X04QC32IIACT
LACTIC ACID, UNSPECIFIED FORM33X04XA5ATIACT
COMMIPHORA MADAGASCARIENSIS RESINWCM0X628RYIACT

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
f29384e1-4418-4fe5-acc9-735adfd9df9c7e76ee98-6483-4d3f-9f5a-c524abf014862025-07-28WarningsExact identifier
spl id: f29384e1-4418-4fe5-acc9-735adfd9df9c
spl set id: 7e76ee98-6483-4d3f-9f5a-c524abf01486

Reported adverse events (FAERS/openFDA)#

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