Age Defense Mineral Moisturizer SPF 30

Manufacturer
Shaklee Corporation
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:22

Label at a glance#

ProductAge Defense Mineral Moisturizer SPF 30
Active ingredientTITANIUM DIOXIDE
Label structure7 sections

Dosage and administration

Apply generously 15 minutes before sun exposure Children under 6 months of age: Ask a doctor 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 s...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 4.2%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

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. Rince with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply generously 15 minutes before sun exposure
  • Children under 6 months of age: Ask a doctor
  • 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:
  1. limit time in the sun, especially from 10 a.m. - 2 p.m.
  2. Wear long-sleeved shirts, pants, hats, and sunglasses
  • Reapply at least every 2 hours
  • Use a water-resistant sunscreen if swimming or sweating

Other Information

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT SECTION

Water (Aqua), Glyverin, Dimethicone, Pentylene Glycol, Ethylhexyl Methoxycrylene, Polyester-8, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyclyceryl-3 Polydimethylciloxyethyl Dimethicone, Squalane, Alumina, Phenoxyethanol, Enteromorpha Compressa (Green Algae) Extract, Polysorbate 60, Eugenia Caryophyllus (Clove) Leaf Oil, Hydrogen Dimethicone, Pisum Sativum (Pea) Extract, Carthamus Tinctorius (Safflower) Seed Oil, Ethylhexylglycerin, Acacia Decurrens Extract, Butylene Glycol, Caesalpinia Spinosa (Tara Tree) Gum, Vitis Rotundifolia (muscadine Grape) Fruis Extract, Tagetes Erecta Flower Extract, Cananga Odorata Flower Oil, Citric Acid, Alteromonas Ferment Extract Magnesium Ascorbyl Phosphate (Vitamin C), Panthenol (Vitamin B5), Coriandrum Sativum (Coriander) Fruit Oil, Vitis Vinifera (Grape) Seed Extract, 1,2-Hexanediol, Beta-Glucan, Caprylyl Glycol, Superoxide Dismutase.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mL NDC: 59899-051-0150 mL NDC: 59899-051-0150 mL NDC: 59899-051-0150 mL NDC: 59899-051-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59899-051-022022-01-28C16284748780-1d6a99b39-8d9f-a426-e053-dadaa90af4c2a70bcc1b-6c88-703f-e053-2995a90aaa52

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59899-051-01Age Defense Mineral Moisturizer SPF 3050 mL in 1 TUBELOTION501
59899-051-02Age Defense Mineral Moisturizer SPF 301 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59899-051AGE DEFENSE MINERAL MOISTURIZER SPF 30 (TITANIUM DIOXIDE) LOTION [SHAKLEE CORPORATION]1Legacy NDC, 2 package rows20200607_a70bcc1b-6c88-703f-e053-2995a90aaa52.zip

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59899-05159899-051-01, 59899-051-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
a70bcc1b-6c89-703f-e053-2995a90aaa52a70bcc1b-6c88-703f-e053-2995a90aaa522020-06-01WarningsExact identifier
spl id: a70bcc1b-6c89-703f-e053-2995a90aaa52
spl set id: a70bcc1b-6c88-703f-e053-2995a90aaa52

Reported adverse events (FAERS/openFDA)#

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