NUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY SPF 30- zinc oxide cream

NUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY SPF 30 by

Drug Labeling and Warnings

NUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY SPF 30 by is a Otc medication manufactured, distributed, or labeled by NUORI ApS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide 20%

Purpose: Sunscreen

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

Warnings

For external use only

Do not use on damaged or broken skin.

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

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

Stop use and ask a doctor if rash occurs.

Directions

• 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

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

• 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?

send them to info@nuori.com

Company Information

MANUFACTURED IN ITALY FOR NUORI ApS

STORMGADE 35/ DK-1555 COPENHAGEN

NUORI.COM/ @NUORISKINCARE

Product Packaging

NUORI

SUN

MINERAL DEFENCE SUNSCREEN

FACE & BODY

HIGH PROTECTION

BROAD SPECTRUM SPF 30

UVA & UVB

FRESH SKINCARE

150ml 5.1fl oz

INGREDIENTS AND APPEARANCE

NUORI MINERAL DEFENCE SUNSCREEN FACE AND BODY SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72894-063
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
BETA CAROTENE (UNII: 01YAE03M7J)
ISOSTEARIC ACID (UNII: X33R8U0062)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
KARUM SEED OIL (UNII: 62160PU6FJ)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CARROT SEED OIL (UNII: 595AO13F11)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
WATER (UNII: 059QF0KO0R)
CARROT (UNII: L56Z1JK48B)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BENZYL ALCOHOL (UNII: LKG8494WBH)
TOCOPHEROL (UNII: R0ZB2556P8)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
MALIC ACID (UNII: 817L1N4CKP)
SHEA BUTTER (UNII: K49155WL9Y)
PROPANEDIOL (UNII: 5965N8W85T)
CETYL ALCOHOL (UNII: 936JST6JCN)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
PASSIFLORA EDULIS FRUIT (UNII: 602YE42W5R)
DOCOSANOL (UNII: 9G1OE216XY)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72894-063-01	1 in 1 CARTON	04/01/2020
1		150 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/01/2020

Labeler - NUORI ApS (305146468)