Label: JACK BLACK SUN GUARD SUNSCREEN SPF45- sunscreen lotion
- NDC Code(s): 66738-304-14, 66738-304-27
- Packager: Jack Black, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 8, 2023
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- Active Ingredients
- Uses
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- Reapply: after 80 minutes of swimming or sweating
- Immediately after towel drying
- At least every two hours
- Children under 6 months: ask a doctor
- Spending time in the sun increases your risk of skin cancer and early skin aging.
- To decrease this risk, regularly use sunscreen with a broad spectrum SFP value of 15 or higher
- Limit time in the sun, eespecially from 10 a.m. - 2 p.m.
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Inactive Ingredients
Artemisia Umbelliformis Extract, Ascorbyl Palmitate, Buddleja Davidii Leaf Extract, Butylene Glycol, Calendula Officinalis Flower Extract, Cyclopentasiloxane, Dimethicone, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Ethylhexyl Isononanoate, Glycerin, Iodopropynyl Butylcarbamate, Lauryl PEG-9 Polymethylsiloxethyl Dimethicone, Leontopodium Aloinum (Edelweiss) Extract, Penoxyethanol, Peucedanum Ostruthium Leaf Extract, Retinyl Palmitate, Sodium Chloride, Triethoxycaprylylsilane, Water
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INGREDIENTS AND APPEARANCE
JACK BLACK SUN GUARD SUNSCREEN SPF45
sunscreen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66738-304 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3 g in 1000 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 1000 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 8 g in 1000 g Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ASCORBYL PALMITATE (UNII: QN83US2B0N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) LEONTOPODIUM ALPINUM FLOWER (UNII: MWN6IZU3XM) PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y) BUDDLEJA DAVIDII LEAF (UNII: X380815D32) ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color white (off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66738-304-14 113 g in 1 TUBE; Type 0: Not a Combination Product 02/09/2010 2 NDC:66738-304-27 44 g in 1 TUBE; Type 0: Not a Combination Product 02/04/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/09/2010 Labeler - Jack Black, LLC (847024036)
