FDA.reportPublic FDA data

NUORI X BOOST THE LIGHT SALON MINERAL DEFENCE SUNSCREEN SPF 30

Manufacturer
The Light Salon Boost Limited
Effective date
2022-01-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:15:56

Label at a glance#

ProductNUORI X BOOST THE LIGHT SALON MINERAL DEFENCE SUNSCREEN SPF 30
Active ingredientZINC OXIDE
Label structure9 sections

Indications and uses

Helps prevent sunburn Higher SPF gives more sunburn protection If used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

Apply liberally on clean, moisturized skin 15 minutes before sun exposure. Reapply at least every 2 hours. For daily use, allow product to absorb completely before applying makeup. Use a water resistant sunscreen if swimming or sweating. 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 a Broad Spectrum ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 23%

Purpose: Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • Higher SPF gives more sunburn protection
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

Directions

INSTRUCTIONS FOR USE SECTION

  • Apply liberally on clean, moisturized skin 15 minutes before sun exposure.
  • Reapply at least every 2 hours.
  • For daily use, allow product to absorb completely before applying makeup.
  • Use a water resistant sunscreen if swimming or sweating.
  • 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • Limit time in the sun, especially from 10 a.m.-2 p.m.
  • Wear long-sleeved shirts, pants, hats and sunglasses.
  • Children under 6 months: Ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), caprylic/capric triglyceride, caprylyl cap rylate/cap rate, glycerin, silica, arachidyl alcohol, cetearyl alcohol, pongamia glabra (karanja) seed oil, helianthus annuus (sunflower) seed oil, daucus carota sativa (carrot) seed oil, daucus carota sativa (carrot) root extract, pinus pinaster (French maritime pine) bark extract, cetearyl olivate, sorbitan olivate, glyceryl oleate, microcrystalline cellulose, behenyl alcohol, arachidyl glucoside, coco-glucoside, lecithin, polyglyceryl-3 polyricinoleate, hydrogenated palm glycerides citrate, polyhydroxystearic acid, isostearic acid, tocopheryl acetate (vitamin E), ascorbyl palmitate, tocopherol (vitamin E), beta-carotene, glucose, xanthan gum, cellulose gum, citric acid, sodium chloride, hydroxyacetophenone, benzyl alcohol.

Other information

OTHER SAFETY INFORMATION

  • Protect the product in this container from excessive heat and direct sun
  • You may report a serious adverse reaction to: NUORI Inc., 228 Park Ave S, Ste 300, New York, NY 10003

Questions?

OTC - QUESTIONS SECTION

send them to info@nuori.com

Company Information

SPL UNCLASSIFIED SECTION

MANUFACTURED IN ITALY FOR NUORI ApS

STORMGADE 35/ DK-1555 COPENHAGEN

NUORI.COM/ @NUORISKINCARE

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NUORI

x

BOOST

THE LIGHT SALON

MINERAL DEFENCE SUNSCREEN

HIGH PROTECTION

BROAD SPECTRUM / SPF 30

UVA & UVB

FRESH SKINCARE

START USING

50ml 1.7 fl oz

mineral defensemineral defense

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73339-17373339-173-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Name, UNII, Kind table
NameUNIIKind
BETA CAROTENE01YAE03M7JIACT
SODIUM CHLORIDE451W47IQ8XIACT
ISOSTEARIC ACIDX33R8U0062IACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
XANTHAN GUMTTV12P4NEEIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
KARUM SEED OIL62160PU6FJIACT
SORBITAN OLIVATEMDL271E3GRIACT
DOCOSANOL9G1OE216XYIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
SUNFLOWER OIL3W1JG795YIIACT
CARROT SEED OIL595AO13F11IACT
MARITIME PINE50JZ5Z98QYIACT
ZINC OXIDESOI2LOH54ZACTIB
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
WATER059QF0KO0RIACT
CAPRYLYL CAPRYLATE/CAPRATE22MCG4RSMRIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
CARROTL56Z1JK48BIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETEARYL OLIVATE58B69Q84JOIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
COCO GLUCOSIDEICS790225BIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ASCORBYL PALMITATEQN83US2B0NIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOOLEATEC4YAD5F5G6IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
BENZYL ALCOHOLLKG8494WBHIACT
TOCOPHEROLR0ZB2556P8IACT

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
d5ca6ae0-85e7-a26b-e053-2a95a90af15990938d3a-2c52-524c-e053-2995a90a07452022-01-17WarningsExact identifier
spl id: d5ca6ae0-85e7-a26b-e053-2a95a90af159
spl set id: 90938d3a-2c52-524c-e053-2995a90a0745

Reported adverse events (FAERS/openFDA)#

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