LIPID SHIELD SPF 30- zinc oxide cream

Lipid Shield SPF 30 by

Drug Labeling and Warnings

Lipid Shield SPF 30 by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Zinc Oxide 21%

PURPOSE

Purpose: Sunscreen

INDICATIONS & USAGE

Uses Helps prevent sunburn and damage caused by UVA/UVB exposure 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

.

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

When using this product In the event of contact with eyes, rinse thoroughly with water

STOP USE

Stop use and ask a doctor if Rash or irritation occurs

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions Apply liberally on dry skin following your morning routine at least 15 minutes before sun exposure For topical use only Keep out of reach of children Children under 6 months: 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 30 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. Reapply to dry skin: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

OTHER SAFETY INFORMATION

Other Information Protect the product in this container from excessive heat and direct sun. May stain some fabrics.

INACTIVE INGREDIENT

Inactive Ingredients: Water (Aqua), Caprylic/Capric Triglyceride, Cetearyl Alcohol, Coconut Alkanes, Glycerin, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Glyceryl Caprylate, Coco-Glucoside, Phaeodactylum Tricornutum Extract, Butyrospermum Parkii (Shea) Butter, Helianthus Annuus (Sunflower) Seed Oil, Disodium Tetramethylhexadecenyl Succinoyl Cysteine, Oryza Sativa Starch, Bisabolol, Dipotassium Glycyrrhizinate, Sodium Phytate, Xanthan Gum, Sclerotium Gum, Cetearyl Glucoside, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin, Dimethicone, Coco-Caprylate/Caprate, Caprylyl/Capryl Glucoside, Caprylhydroxamic Acid, Tocopherol, Beta-Sitosterol, Squalene, Triethoxycaprylylsilane
May Contain: Iron Oxide (CI 77491, CI77492, CI77499)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIPID SHIELD SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4273
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	21 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
TOCOPHEROL (UNII: R0ZB2556P8)
PHAEODACTYLUM TRICORNUTUM (UNII: Y5W63E7HLV)
SHEA BUTTER (UNII: K49155WL9Y)
DISODIUM TETRAMETHYLHEXADECENYL SUCCINOYL CYSTEINE (UNII: CZA8L664YS)
COCONUT ALKANES (UNII: 1E5KJY107T)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
CI 77499 (UNII: XM0M87F357)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
COCO-GLUCOSIDE (UNII: ICS790225B)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
BISABOLOL (UNII: 24WE03BX2T)
XANTHAN GUM (UNII: TTV12P4NEE)
SCLEROTIUM GUM (UNII: 2X51AD1X3T)
ISOSTEARIC ACID (UNII: X33R8U0062)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
CAPRYLYL/CAPRYL GLUCOSIDE (UNII: E00JL9G9K0)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
.BETA.-SITOSTEROL (UNII: S347WMO6M4)
CI 77492 (UNII: EX438O2MRT)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
ORYZA SATIVA (RICE) STARCH (UNII: 4DGK8B7I3S)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X)
SODIUM PHYTATE (UNII: 88496G1ERL)
DIMETHICONE (UNII: 92RU3N3Y1O)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CI 77491 (UNII: 1K09F3G675)
SQUALENE (UNII: 7QWM220FJH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4273-2	1 in 1 CARTON	08/07/2025
1	NDC: 62742-4273-1	50 g in 1 BOTTLE, PUMP; 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	08/07/2025

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4273)