Drug labels

Jack Black

TITANIUM DIOXIDE, ZINC OXIDE · Jack Black L.L.C · TOPICAL

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
181d5bf3-ce91-cb2c-e063-6294a90a51c4
ID
181d5bf3-ce92-cb2c-e063-6294a90a51c4
Effective time
20240510
Version
1
SPL product data elements

Jack Black Titanium Dioxide, Zinc Oxide DECAMETHYLTETRASILOXANE HYDROGENATED SOYBEAN LECITHIN HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) ROSEMARY WATER ALUMINUM OXIDE NIACINAMIDE AZELAIC ACID MEDIUM-CHAIN TRIGLYCERIDES GLYCERIN PROPANEDIOL SORBITAN ISOSTEARATE HYDROGENATED SOYBEAN PHOSPHATIDYLCHOLINE ANHYDROUS CITRIC ACID XANTHAN GUM XYLITOL AMINOMETHYLPROPANOL SILICON DIOXIDE PHENOXYETHANOL TRIETHOXYCAPRYLYLSILANE HYALURONATE SODIUM TITANIUM DIOXIDE TITANIUM DIOXIDE POLYHYDROXYSTEARIC ACID (2300 MW) PEG-60 SORBITAN STEARATE GREEN TEA LEAF ZINC OXIDE ZINC OXIDE RICE GERM ALLANTOIN BUTYLOCTYL SALICYLATE ISOHEXADECANE CRANBERRY STEARIC ACID

Active ingredient
Active Ingredient Titanium Dioxide 3.9% Zinc Oxide 3.2%
Purpose
Purpose Sunscreen
Indications and usage
Use Helps prevent sunburn
Warnings
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 product is swallowed, get medical help or contact a Poison Control Center right away
Dosage and administration

Directions • 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.

Storage and handling
Other Information ■ Protect the product in this container from excessive heat and direct sun
Inactive ingredient

Inactive Ingredients Water, Caprylic/Capric Triglyceride, Glycerin, Butyloctyl Salicylate, Propanediol, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Silica, Azelaic Acid, Allantoin, Sodium Hyaluronate, Camellia Sinensis Leaf Extract*, Vaccinium Macrocarpon (Cranberry) Fruit Extract*, Rosmarinus Officinalis (Rosemary) Leaf Extract*, Niacinamide, Oryza Sativa (Rice) Extract, Alumina, Isohexadecane, Hydrogenated Lecithin, Polyhydroxystearic Acid, Xylitol, Stearic Acid, Polysorbate 60, Triethoxycaprylylsilane, Xanthan Gum, Aminomethyl Propanol, Sorbitan Isostearate, Hydrogenated Phosphatidylcholine, Citric Acid, Phenoxyethanol. 24012 *Certified Organic

Questions
Questions? www.getJackBlack.com 1-877-766-3388; 1-469-341-2700
Package label principal display panel

Principal Display Panel Jack Black Authentic and Original Dual Defense Face Moisturizer 100% Mineral Sunscreen Broad Spectrum SPF 30 with Hyaluronic Acid & Niacinamide SPF 30 59 mL / 2 FL OZ Jack Black Authentic and Original Dual Defense Face Moisturizer 100% Mineral Sunscreen Broad Spectrum SPF 30 with Hyaluronic Acid & Niacinamide SPF 30 59 mL / 2 FL OZ Jack Black Authentic and Original Dual Defense Face Moisturizer 100% Mineral Sunscreen Broad Spectrum SPF 30 with Hyaluronic Acid & Niacinamide SPF 30 15 mL / 0.5 FL OZ Tube Carton Packet

Harmonized identifiers (openFDA)
Application number
M020
Brand name
Jack Black
Generic name
TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer name
Jack Black L.L.C
Product NDC
66738-502
Product type
HUMAN OTC DRUG
Route
TOPICAL
Substance name
TITANIUM DIOXIDE, ZINC OXIDE
SPL ID
181d5bf3-ce92-cb2c-e063-6294a90a51c4
SPL set ID
181d5bf3-ce91-cb2c-e063-6294a90a51c4
Package NDC
66738-502-22, 66738-502-01, 66738-502-21
Is original packager
true
UNII
15FIX9V2JP, SOI2LOH54Z
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.