NUDA CANADA SOLARGLOW MINERAL SERUM SUNSCREEN SPF30- zinc oxide cream

NUDA CANADA SOLARGLOW MINERAL SERUM SUNSCREEN by

Drug Labeling and Warnings

NUDA CANADA SOLARGLOW MINERAL SERUM SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by LABORATOIRES DRUIDE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredients

Zinc Oxide 13%

Purpose

Sunscreen

Uses

▪ Helps prevent sunburn. ▪ 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.

When using this product

Stop use and ask a doctor if

rash occurs.

Keep out of reach of children

If swallowed, get medical help or contact Poison Control Center right away.

Directions

▪ Apply liberally and evenly 15 minutes before sun exposure ▪ Reapply ▪ After 80 minutes of swimming or sweating ▪ Immediately after towel drying ▪ At least every 2 hours ▪ 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 ▪ Use a water-resistant sunscreen if swimming or sweating.

Other Information

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

Inactive Ingredients

Aqua (Water), C15-19 Alkane, Caprylic/Capric Triglyceride, Coco-Caprylate/Caprate, Argania Spinosa Kernel Oil, Polyglyceryl-6 Polyhydroxystearate, Tocopheryl Acetate, Caprytic/Capric Triglyceride, Amylopectin, Polyglyceryl-6 Polyricinoleate, Polyhydroxystearic Acid, Sorbitan Olivate, Sodium Chloride, Hydrolyzed Jojoba Esters, Jojoba Esters, Benzyl Alcohol, Salicylic Acid, Glycerin, Sorbic Acid, Iron Oxides, Octyldodecanol, Trihydroxystearin, Tocopherol (Vitamin E), Xanthan Gum, Niacinamide, Squalane, Punica Granatum Seed Oil, Linoleic Acid (and Linolenic Acid (Vitamin F), Cocos Nucifera (Coconut) Oil, Bisabolol, Fragrance (Parfum).

Questions or Comments?

Call 1.833.993-NUDA
or visit www.nuda.ca

NUDA CANADA SOLARGLOW MINERAL SERUM SUNSCREEN SPF30 50mL (NDC:

71447-057-00)

INGREDIENTS AND APPEARANCE

NUDA CANADA SOLARGLOW MINERAL SERUM SUNSCREEN  SPF30
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71447-058
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
C15-19 ALKANE (UNII: CI87N1IM01)
OCTYLDODECANOL (UNII: 461N1O614Y)
NIACINAMIDE (UNII: 25X51I8RD4)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
JOJOBA OIL (UNII: 724GKU717M)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
PUNICA GRANATUM SEED OIL (UNII: 0UI45XV0T6)
LINOLEIC ACID (UNII: 9KJL21T0QJ)
POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
SORBITAN OLIVATE (UNII: MDL271E3GR)
SQUALANE (UNII: GW89575KF9)
CAPRYLIC/CAPRIC/LINOLEIC TRIGLYCERIDE (UNII: U73D397055)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO-CAPRYLATE (UNII: 4828G836N6)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SORBIC ACID (UNII: X045WJ989B)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
LEVOMENOL (UNII: 24WE03BX2T)
COCOS NUCIFERA WHOLE (UNII: 245J88W96L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71447-058-01	1 in 1 BOX	11/20/2023
1	NDC: 71447-058-00	50 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 Drug	M020	11/20/2023

Labeler - LABORATOIRES DRUIDE INC (245815014)

Registrant - LABORATOIRES DRUIDE INC (245815014)

Establishment
Name	Address	ID/FEI	Business Operations
LABORATOIRES DRUIDE INC		245815014	manufacture(71447-058)