ALOE UP SPF 50 MINERAL- zinc oxide, titanium dioxide spray

Aloe Up SPF 50 Mineral by

Drug Labeling and Warnings

Aloe Up SPF 50 Mineral by is a Otc medication manufactured, distributed, or labeled by Aloe Care International, LLC, Inspec Solutions, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc: 19.5%

Titanium: 4.0%

PURPOSE

Sunscreen

INDICATIONS & USAGE

• helps prevent sunburn
• is 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. Keep away from face to avoid breathing it. Contents under pressure - do not puncture or incinerate. Do not store at temperatures about 120°F.

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get miedical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

• Spray liberally and spread evenly by hand 15 minutes before sun exposure.
• Hold container 4 to 6 inches from skin to apply
• Do not spray directly into face. Spray on hands then apply to face
• Do not apply in windy conditions
• Use in a well-ventilated area
• 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 broad spectrum SPF of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 am - 2 pm
• Wear long-sleeve shirts, pants, hats, and sunglasses
• Children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

• Protect the product from excessive heat and direct sun.
• Avoid spraying on fabrics - could cause discoloration
• Store at 20° to 25°C (68° to 77°F)

INACTIVE INGREDIENT

Aloe Barbadensis Leaf Juice

Caprylic/Capric Triglyceride

Caprylyl Glycol

Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Demethicone

Fragrance

Dimethicone

Ethylhexylglycerin

Glycerin

Hydronated Polydecence

Isopropyl Myristate

Jojoba Esters

Pentylene Glycol

Polyhydroxystearic Acid

Propanediol

Silica

Sodium Chloride

Sodium Phytate

Sorbitan Olivate

Stearic Acid

Synthetic Beeswax

Water

Tetrafluoropropene

QUESTIONS

Questions or Comments?

Call toll free 1-800-950-2563

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALOE UP SPF 50 MINERAL 
zinc oxide, titanium dioxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61477-232
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	19.5 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPANEDIOL (UNII: 5965N8W85T)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHYTATE (UNII: 88496G1ERL)
SORBITAN OLIVATE (UNII: MDL271E3GR)
STEARIC ACID (UNII: 4ELV7Z65AP)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
WATER (UNII: 059QF0KO0R)
2,3,3,3-TETRAFLUOROPROPENE (UNII: P5N89242X3)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
CETYL DIGLYCERYL TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE (950 MM2/S) (UNII: C982F2EKT3)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61477-232-01	128 g in 1 CAN; Type 0: Not a Combination Product	05/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/22/2025

Labeler - Aloe Care International, LLC (938242187)

Registrant - Inspec Solutions, LLC (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions, LLC		081030372	manufacture(61477-232)