TRUSKIN BROAD SPECTRUM MINERAL SUNSCREEN FACIAL SERUM WITH VITAMIN C AND ALOE- zinc oxide cream

Truskin Broad Spectrum Mineral Sunscreen Facial Serum with Vitamin C and Aloe by

Drug Labeling and Warnings

Truskin Broad Spectrum Mineral Sunscreen Facial Serum with Vitamin C and Aloe by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Zinc Oxide 16.1%

PURPOSE

Purpose: Sunscreen

INDICATIONS & USAGE

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

Do not use on damaged or broken skin.

WHEN USING

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

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions ■ Shake well before use ■ Apply generously 15 minutes before sun exposure ■ Reapply at least every 2 hours ■ 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 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 of age: Ask a doctor.

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun. May stain some fabrics.

INACTIVE INGREDIENT

Inactive Ingredients:
Water(Aqua),Caprylic/capric Triglyceride, Isopropyl Isostearate, Polyglyceryl -4 Diisostearate/Polyhydroxy stearate/sebacate, Coconut Alkanes, C13-15 Alkane, Glycerin, Sodium Chloride, Maltodextrin, Phenoxyethanol, Xanthan Gum, Polyhydroxystearic acid, Polyglyceryl – 3 Polyricinoleate, Isosteric acid, Lecithin, Caprylyl Glycol, Coco-Caprylate/-Caprate, Ethylhexylglycerin, Hexylene Glycol, Sodium Ascorbyl Phosphate, Caesalpinia Spinosa Fruit Pod Extract, Opuntia Ficus-Indica Stem Extract, Niacinamide, Helianthus Annuus ( Sunflower) Sprout Extract,Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Sodium Hyaluronate, Sodium Benzoate, Citric Acid, Potassium Sorbate, May Contain +/_ Iron oxides ( CI77491, CI77492, CI 77499)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRUSKIN BROAD SPECTRUM MINERAL SUNSCREEN FACIAL SERUM WITH VITAMIN C AND ALOE 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4275
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	16.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
NIACINAMIDE (UNII: 25X51I8RD4)
WATER (UNII: 059QF0KO0R)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
CI 77492 (UNII: EX438O2MRT)
C13-15 ALKANE (UNII: 114P5I43UJ)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CAESALPINIA SPINOSA FRUIT POD (UNII: EXY4496LWD)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W)
CI 77491 (UNII: 1K09F3G675)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ISOSTEARIC ACID (UNII: X33R8U0062)
CITRIC ACID (UNII: 2968PHW8QP)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GLYCERIN (UNII: PDC6A3C0OX)
CI 77499 (UNII: XM0M87F357)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
COCONUT ALKANES (UNII: 1E5KJY107T)
OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4275-2	1 in 1 CARTON	11/06/2025
1	NDC: 62742-4275-1	30 g in 1 BOTTLE, PUMP; 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	11/06/2025

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4275)