LIFTINTENSE SCULPTING WITH MINERAL BROAD SPECTRUM SPF 15 SUNSCREEN- zinc oxide cream

LiftIntense Sculpting with Mineral Broad Spectrum SPF 15 Sunscreen by

Drug Labeling and Warnings

LiftIntense Sculpting with Mineral Broad Spectrum SPF 15 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Arbonne International, LLC, Levlad, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Zinc oxide 8%

Purpose

Sunscreen

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

For external use only

Do not useon damaged or broken skin

When using this productkeep out of eyes. Rinse with water to remove.

Stop use and ask a doctor ifrash occurs.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

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
• 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

• protect the product in this container from excessive heat and direct sun

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.

Questions or comments?

1-800-272-6663

Monday–Friday 6 a.m.–6 p.m. PST

SPL UNCLASSIFIED SECTION

Distributed by Arbonne International, LLC Greenwood, IN 46143 USA

PRINCIPAL DISPLAY PANEL - 50 g Jar Carton

100% VEGAN – CRUELTY-FREE

LiftIntense

SCULPTING CREAM
WITH MINERAL BROAD SPECTRUM
SPF 15 SUNSCREEN

All Skin Types

Net wt. 1.7 oz. / 50 g

INGREDIENTS AND APPEARANCE

LIFTINTENSE SCULPTING WITH MINERAL BROAD SPECTRUM SPF 15 SUNSCREEN 
zinc oxide cream

Product 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)