Aloe Up SPF 50 Mineral Spray 4.5 oz

Manufacturer
Aloe Care International, LLC | Inspec Solutions, LLC
Effective date
2025-06-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:03:24

Label at a glance#

ProductAloe Up SPF 50 Mineral
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc: 19.5%

Titanium: 4.0%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

  • 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 SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • 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 SECTION

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

OTC - QUESTIONS SECTION

Questions or Comments?

Call toll free 1-800-950-2563

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aloe UP SPF 50 Mineral SprayAloe UP SPF 50 Mineral Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61477-232-01Aloe Up SPF 50 Mineral128 g in 1 CANSPRAY1283

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61477-23261477-232-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
Aloe Up SPF 50 MineralZINC OXIDE, TITANIUM DIOXIDEAloe Care International, LLC35b9dcfa-05f3-3d7b-e063-6394a90a18f12025-06-18WarningsExact identifier
ndc (package): 61477-232-01
ndc (product): 61477-232
ndc11 (package): 61477023201
spl id: 37d95f06-6460-88da-e063-6394a90a6dcd
spl set id: 35b9dcfa-05f3-3d7b-e063-6394a90a18f1

Reported adverse events (FAERS/openFDA)#

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