Label: JACK BLACK- titanium dioxide, zinc oxide lotion
- NDC Code(s): 66738-502-01, 66738-502-21, 66738-502-22
- Packager: Jack Black L.L.C
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 10, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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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.
- Other Information
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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?
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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
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INGREDIENTS AND APPEARANCE
JACK BLACK
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-502 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3.9 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3.2 g in 100 mL Inactive Ingredients Ingredient Name Strength DECAMETHYLTETRASILOXANE (UNII: C23WAL597T) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) ROSEMARY (UNII: IJ67X351P9) WATER (UNII: 059QF0KO0R) ALUMINUM OXIDE (UNII: LMI26O6933) NIACINAMIDE (UNII: 25X51I8RD4) AZELAIC ACID (UNII: F2VW3D43YT) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) HYDROGENATED SOYBEAN PHOSPHATIDYLCHOLINE (UNII: QHQ97HF0PY) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) XANTHAN GUM (UNII: TTV12P4NEE) XYLITOL (UNII: VCQ006KQ1E) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) HYALURONATE SODIUM (UNII: YSE9PPT4TH) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) PEG-60 SORBITAN STEARATE (UNII: 073G38N8GC) GREEN TEA LEAF (UNII: W2ZU1RY8B0) RICE GERM (UNII: 7N2B70SFEZ) ALLANTOIN (UNII: 344S277G0Z) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ISOHEXADECANE (UNII: 918X1OUF1E) CRANBERRY (UNII: 0MVO31Q3QS) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-502-01 1 in 1 CARTON 07/31/2024 1 NDC:66738-502-22 59 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:66738-502-21 14 mL in 1 PACKET; Type 0: Not a Combination Product 07/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/31/2024 Labeler - Jack Black L.L.C (847024036) Establishment Name Address ID/FEI Business Operations Pure Source L.L.C 080354456 manufacture(66738-502)