Label: LIFTINTENSE SCULPTING WITH MINERAL BROAD SPECTRUM SPF 15 SUNSCREEN- zinc oxide cream
- NDC Code(s): 42508-791-23
- Packager: Arbonne International, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
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Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
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Directions
For sunscreen use:
- apply liberally and evenly 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- children under 6 months of age: Ask a doctor
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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, butyloctyl salicylate, pentaerythrityl isostearate/caprate/caprylate/adipate, glycerin, cetearyl alcohol, steareth-21, steareth-2, squalane, dicetyl phosphate, caprylyl glycol, ceteth-10 phosphate, pyrus malus (apple) fruit extract, hydrolyzed pea protein, paeonia albiflora root extract, undaria pinnatifida extract, tetrahexyldecyl ascorbate, tocopherol, sodium hyaluronate, acetyl tetrapeptide-2, ethylhexylglycerin, polyhydroxystearic acid, xanthan gum, hexylene glycol, sodium phytate, citric acid, sodium citrate, alcohol, phenoxyethanol, potassium sorbate.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 g Jar Carton
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INGREDIENTS AND APPEARANCE
LIFTINTENSE SCULPTING WITH MINERAL BROAD SPECTRUM SPF 15 SUNSCREEN
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42508-791 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 80 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARETH-21 (UNII: 53J3F32P58) STEARETH-2 (UNII: V56DFE46J5) SQUALANE (UNII: GW89575KF9) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) APPLE (UNII: B423VGH5S9) PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ACETYL TETRAPEPTIDE-2 (UNII: M24S4WZS8J) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE) XANTHAN GUM (UNII: TTV12P4NEE) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PHYTATE SODIUM (UNII: 88496G1ERL) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42508-791-23 1 in 1 CARTON 06/01/2021 01/24/2025 1 50 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2021 01/24/2025 Labeler - Arbonne International, LLC (961643454) Registrant - Levlad, LLC (076245109)
