LAZY FACE SPF 30 FACESTICK- zinc oxide stick

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 18%

PURPOSE

Sunscreen

INDICATIONS & USAGE

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 use on damaged or broken skin.

When using this product avoid contact with eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

For sunscreen use:
Apply liberally 15 minutes before sun exposure and as needed
Reapply:

After 80 minutes of swimming or sweating Immediately after towel drying
At least every 2 hours

Sun protective 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 10am–2pm. Wear long-sleeved shirts, pants, hats, and sunglasses

Children under 6 months of age: ask a doctor

INACTIVE INGREDIENT

Cetearyl Nonanoate, Caprylic/Capric Triglyceride, Euphorbia Cerifera (Candelilla) Wax, Helianthus Annuus (Sunflower) Seed Wax, Capryloyl Glycerin/Sebacic Acid Copolymer, Butyloctyl Salicylate, Lauryl Laurate, Polyhydroxystearic Acid, Behenyl Behenate, Oryzanol, Butyrospermum Parkii (Shea) Butter, Theobroma Cacao (Cocoa) Seed Butter, Bisabolol, Tocopherol, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LAZY FACE SPF 30 FACESTICK 
zinc oxide stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87619-1833
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	18 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ORYZANOL (UNII: SST9XCL51M)
BISABOLOL (UNII: 24WE03BX2T)
CETEARYL NONANOATE (UNII: F6ZWV2F361)
CANDELILLA WAX (UNII: WL0328HX19)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
LAURYL LAURATE (UNII: GPW77G0937)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
BEHENYL BEHENATE (UNII: K8NU647RJ0)
SHEA BUTTER (UNII: K49155WL9Y)
COCOA BUTTER (UNII: 512OYT1CRR)
TOCOPHEROL (UNII: R0ZB2556P8)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
SOYBEAN LECITHIN (UNII: 1DI56QDM62)
SORBITAN OLIVATE (UNII: MDL271E3GR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87619-1833-1	1 in 1 CARTON	04/22/2026
1		14 g in 1 VIAL, PLASTIC; 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	04/22/2026

Labeler - Sunny Day Creations (135234902)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(87619-1833)