Jack Black Dual Defense Face Moisturizer - SPF 30

Manufacturer
Jack Black L.L.C | Pure Source L.L.C
Effective date
2024-05-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:02:58

Label at a glance#

ProductJack Black Dual Defense Face Moisturizer - SPF 30
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure13 sections

Dosage and administration

• Apply liberally 15 minutes before sun exposure • Children under 6 months of age: Ask a doctor • 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 a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 3.9%.

Zinc Oxide 3.2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn

Warnings

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.

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 medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Caprylic/Capric Triglyceride, Glycerin, Butyloctyl Salicylate, Propanediol, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Azelaic Acid, Allantoin, Sodium Hyaluronate, Camellia Sinensis Leaf Extract*, Rosmarinus Officinalis (Rosemary) Leaf Extract*, Vaccinium Macrocarpon (Cranberry) Fruit Extract*, Silica, Alumina, Isohexadecane, Hydrogenated Lecithin, Polyhydroxystearic Acid, Xylitol, Stearic Acid, Niacinamide, Polysorbate 60, Oryza Sativa (Rice) Extract, Triethoxycaprylylsilane, Xanthan Gum, Aminomethyl Propanol, Sorbitan Isostearate, Hydrogenated Phosphatidylcholine, Methicone, Citric Acid, Phenoxyethanol. 21002 *Certified Organic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dual Defense 09-2050-01 2 oz tubeDual Defense 09-2050-01 2 oz tubeDual Defense Carton 2 ozDual Defense Carton 2 oz

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66738-501JACK BLACK DUAL DEFENSE FACE MOISTURIZER - SPF 30 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [JACK BLACK L.L.C]2Legacy NDC20240511_eac292fe-b255-39dd-e053-2a95a90a1323.zip

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66738-50166738-501-21, 66738-501-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 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
181d49e7-9fae-9a75-e063-6294a90a7690eac292fe-b255-39dd-e053-2a95a90a13232024-05-10WarningsExact identifier
spl id: 181d49e7-9fae-9a75-e063-6294a90a7690
spl set id: eac292fe-b255-39dd-e053-2a95a90a1323

Reported adverse events (FAERS/openFDA)#

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