FDA.reportPublic FDA data

NUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY SPF 30

Manufacturer
NUORI ApS
Effective date
2022-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:48:32

Label at a glance#

ProductNUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY 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 20%

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), coco-caprylate/caprate, caprylic/capric triglyceride, ethyl macadamiate, butyrospermum parkii (shea) butter, propanediol, polyglyceryl-6 polyhydroxystearate, cetyl alcohol, pongamia glabra (karanja) seed oil, polyglyceryl-6 polyricinoleate, sorbitol, arachidyl alcohol, benzyl alcohol, hydroxyacetophenone, helianthus annuus (sunflower) seed oil, behenyl alcohol, hydrolyzed jojoba esters, isostearic acid, lecithin, polyglyceryl-3 polyricinoleate, polyhydroxystearic acid, arachidyl glucoside, sclerotium gum, passiflora edulis (passionfruit) fruit extract, tocopherol (vitamin E), beta-carotene, daucus carota sativa (carrot) root extract, daucus carota sativa (carrot) seed oil, glucose, malic acid, ascorbyl palmitate, citric acid.

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

SUN

MINERAL DEFENCE SUNSCREEN

FACE & BODY

HIGH PROTECTION

BROAD SPECTRUM SPF 30

UVA & UVB

FRESH SKINCARE

150ml 5.1fl oz

NUORINUORI

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72894-06372894-063-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
PASSIFLORA EDULIS FRUIT602YE42W5RIACT
DOCOSANOL9G1OE216XYIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
SORBITOL506T60A25RIACT
LECITHIN, SUNFLOWER834K0WOS5GIACT
KARUM SEED OIL62160PU6FJIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
ETHYL MACADAMIATEANA2NCS6V1IACT
BETA CAROTENE01YAE03M7JIACT
ISOSTEARIC ACIDX33R8U0062IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
SUNFLOWER OIL3W1JG795YIIACT
CARROT SEED OIL595AO13F11IACT
ZINC OXIDESOI2LOH54ZACTIB
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
WATER059QF0KO0RIACT
CARROTL56Z1JK48BIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ASCORBYL PALMITATEQN83US2B0NIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
BENZYL ALCOHOLLKG8494WBHIACT
TOCOPHEROLR0ZB2556P8IACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
BETASIZOFIRAN2X51AD1X3TIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
MALIC ACID817L1N4CKPIACT
SHEA BUTTERK49155WL9YIACT
PROPANEDIOL5965N8W85TIACT
CETYL ALCOHOL936JST6JCNIACT

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
ed244736-9056-77b4-e053-2995a90a4d259dd8339b-7870-0e23-e053-2995a90ac5f62022-11-10WarningsExact identifier
spl id: ed244736-9056-77b4-e053-2995a90a4d25
spl set id: 9dd8339b-7870-0e23-e053-2995a90ac5f6

Reported adverse events (FAERS/openFDA)#

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