Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32

Manufacturer
Allure Labs Inc
Effective date
2020-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:08:54

Label at a glance#

ProductDaily SPF Facial SunscreenLotion Broad Spectrum SPF 32
Active ingredientZINC OXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Zinc Oxide 21%

OTC - PURPOSE SECTION

Purpose: Sunscreen

INDICATIONS & USAGE SECTION

Uses:

  • Helps prevent sunburn. If used as directed with other sun protection measures (see Direction), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS AND PRECAUTIONS SECTION

Warning: For external use only.

OTC - DO NOT USE SECTION

Do not use: on damaged or broken skin.

OTC - WHEN USING SECTION

When using this products: Keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor: If rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions:

Apply generously 15 minutes before sun exposer. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. 

Sun protection measures: Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF 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.

OTHER SAFETY INFORMATION

Other Information: Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Caprylyc/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Tocopheryl Acetate, Helianthus annuus (sunflower) seed oil, Coco-Glucoside, Glyceryl Caprylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside, Xanthan Gum, Coco-Caprylate/Caprate, Lecithin, Caprylyl/Capryl Glucoside, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Oryza Sativa Starch, Dipotassium Glycyrrhizate, Bisabolol, Caprylhydroxamic Acid, Sodium Pthalate, Sclerotium Gum, Sucrose, Phaeodactylum Tricornutum Extract, Glucose, Spirulina Maxima Extract, Tocopherol, C10 Alochol, C8 Alcohol. 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Distributed by 

Onekind.25 Inc

San Francisco, CA 94107 USA

www.cocokind.com

Image SPF32Image SPF32

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62742-419262742-4192-1, 62742-4192-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a09f6a61-08e1-4e5c-9562-cf6eb866e85ba8d172a4-d11f-4b3f-a407-1f08dfd0a1582020-11-02WarningsExact identifier
spl id: a09f6a61-08e1-4e5c-9562-cf6eb866e85b
spl set id: a8d172a4-d11f-4b3f-a407-1f08dfd0a158

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.