Label: SPIT AND POLISH MINERAL LIP BALM BROAD SPECTRUM LIP PROTECTANT SPF 30- zinc oxide stick
- NDC Code(s): 80325-002-01
- Packager: Naturally Uncommon, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 9, 2023
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- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredients
- 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 2 hours.
Sun protection measures
Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures.
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INACTIVE INGREDIENTS:
Prunus Amygdalus Dulcis (Almond) Oil, Butyrospermum Parkii (Shea) Butter, Cera Alba (Beeswax), Simmondsia Chinensis (Jojoba) Seed Oil, Euphorbia Cerifera (Candelilla) Wax, DL-Alpha-Tocopheryl Acetate, Argania Spinosa Kernel (Argan) Oil, Copernicia Cerifera (Carnauba) Wax, Bisabolol, Glyceryl Caprylate, Glyceryl Undecylenate, Triethoxycaprylylsilane
- Package Labeling:
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INGREDIENTS AND APPEARANCE
SPIT AND POLISH MINERAL LIP BALM BROAD SPECTRUM LIP PROTECTANT SPF 30
zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80325-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 80 mg in 1 g Inactive Ingredients Ingredient Name Strength ALMOND (UNII: 3Z252A2K9G) SHEA BUTTER (UNII: K49155WL9Y) YELLOW WAX (UNII: 2ZA36H0S2V) JOJOBA OIL (UNII: 724GKU717M) CANDELILLA WAX (UNII: WL0328HX19) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) ARGAN OIL (UNII: 4V59G5UW9X) CARNAUBA WAX (UNII: R12CBM0EIZ) LEVOMENOL (UNII: 24WE03BX2T) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80325-002-01 4.25 g in 1 APPLICATOR; Type 0: Not a Combination Product 03/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/01/2020 Labeler - Naturally Uncommon, LLC (044473410)