LEADERS SUNBUDDY DAILY MOISTURE SUNSCREEN

Manufacturer
LEADERS COSMETICS CO.,LTD.
Effective date
2017-02-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:53

Label at a glance#

ProductLEADERS SUNBUDDY DAILY MOISTURE SUNSCREEN
Active ingredientHomosalate, Octocrylene, Octisalate, Avobenzone
Label structure6 sections

Dosage and administration

Directions: Take an appropriate amount and apply thinly to the face and neck which is likely to be exposed to UV rays at the final stage of skin care. Finish by tapping lightly. Apply liberally 15 min before sun exposure. Reapply after 40min of swimming or sweating.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Homosalate 9.5%, Octocrylene 5.0%, Ethylhexyl Salicylate 4.5%, Butyl Methoxydibenzoylmethane 3.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Dipropylene Glycol, Glycerin, Niacinamide, Propanediol, Dimethicone/Vinyl Dimethicone Crosspolymer, Hydrolyzed Wheat Protein/PVP Crosspolymer, Argania SpinosaKernel Oil, Betula Alba Juice, Avena Sativa (Oat) Kernel Extract, Honey Extract, Vanilla Tahitensis Fruit Extract, Portu laca Oleracea Extract, Caprylyl Methicone, Perlite, Dicaprylyl Carbonate, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cetearyl Glucoside, Hydroxyacetophenone, Panthenol, Tocopheryl Acetate, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Dipotassium Glycyrrhizate, Adenosine, Sorbitan Oleate, Isoceteth-10, Isoceteth-25, Sodium Phytate, Ethylhexylglycerin, Butylene Glycol, 1,2-Hexanediol, Cetearyl Alcohol, Xanthan Gum, Disodium EDTA, Phenoxyethanol, Potassium Sorbate, Fragrance(Parfum), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warning: For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DESCRIPTION SECTION

Directions: Take an appropriate amount and apply thinly to the face and neck which is likely to be exposed to UV rays at the final stage of skin care. Finish by tapping lightly. Apply liberally 15 min before sun exposure. Reapply after 40min of swimming or sweating.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809483314213GTIN-13: 8809483314213
EAN-13: 8809483314213
GTIN storage (14 digits): 08809483314213
leaders sunbuddy daily moisture sunscreen carton.jpg
QR code linkQR Codem.site.naver.com/07Xjpleaders sunbuddy daily moisture sunscreen carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69424-580-022020-01-31C16284748780-19d75b9d1-0531-f424-e053-dadaa90a57ceecff440b-c4be-4e64-81f8-e6c82c50b108

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69424-580-01LEADERS SUNBUDDY DAILY MOISTURE SUNSCREEN70 mL in 1 TUBECREAM701
69424-580-02LEADERS SUNBUDDY DAILY MOISTURE SUNSCREEN1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69424-580LEADERS SUNBUDDY DAILY MOISTURE SUNSCREEN (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) CREAM [LEADERS COSMETICS CO.,LTD.]1Legacy NDC, 2 package rows20170222_ecff440b-c4be-4e64-81f8-e6c82c50b108.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69424-58069424-580-01, 69424-580-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
48810fd2-1df9-4eda-87bf-097389bcc732ecff440b-c4be-4e64-81f8-e6c82c50b1082017-02-22WarningsExact identifier
spl id: 48810fd2-1df9-4eda-87bf-097389bcc732
spl set id: ecff440b-c4be-4e64-81f8-e6c82c50b108

Reported adverse events (FAERS/openFDA)#

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