Moonshot Multi Protection UV Bouncer

Manufacturer
Codecosme International Co., Ltd. | Cosmax, Inc.
Effective date
2019-01-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:17

Label at a glance#

ProductMoonshot Multi Protection UV Bouncer
Active ingredientHomosalate, Octocrylene, Octisalate, Avobenzone
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredient:
Water, Alcohol Denat., Butylene Glycol, Acrylates Copolymer, Diphenylsiloxy Phenyl Trimethicone, Methyl Methacrylate Crosspolymer, Pentylene Glycol, Polymethylsilsesquioxane, "Sodium Acrylate/Sodium Acryloyldimethyl, Taurate Copolymer", Isohexadecane, Beheneth-25, Caprylyl Glycol, Fragrance(Parfum), Polysorbate 80, Sorbitan Oleate, Disodium EDTA, Saccharide Isomerate, Xylitylglucoside, Anhydroxylitol, Xylitol, Glucose, Citric Acid, Sodium Citrate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

1. If any of the following symptoms occur when using the product, stop using immediately and consult a dermatologist. a) red spots, swelling, itchy rashes other skin irritations, etc. b) if a) occurs after applying and being exposed to sunlight. 2. Do not use on wounds, inflamed skin, itchy areas, or other infected areas. 3. Storage and handling: a) must close cap after use. b) Keep out of reach of children. c) keep away from extreme heat, cold and direct sunlight. d) Avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water. 4. For external use only.

DESCRIPTION

DESCRIPTION SECTION

Uses:

A cooling and moisturizing UV protector / makeup primer.
Aqua UV cooling protector provides the skin with protection from UV rays and the unique aqua base formula creates a moisturizing, cooling and refreshing effect.

Directions:

Pump appropriate amount of the product onto your hands and apply on the entire face in outward strokes using a sponge or fingertips. Close cap after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71786-060-022021-01-29C16284748780-1ba0f9c33-2e0e-a910-e053-dadaa90a0b85943e9f7f-ec0e-483a-9171-0cd64f93618c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71786-060-01Moonshot Multi Protection UV Bouncer40 mL in 1 CONTAINERCREAM401
71786-060-02Moonshot Multi Protection UV Bouncer1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71786-060MOONSHOT MULTI PROTECTION UV BOUNCER (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) CREAM [CODECOSME INTERNATIONAL CO., LTD.]1Legacy NDC, 2 package rows20190122_943e9f7f-ec0e-483a-9171-0cd64f93618c.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
71786-06071786-060-01, 71786-060-02

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
f5322af7-72d0-430a-a3b3-6fd09c2f088a943e9f7f-ec0e-483a-9171-0cd64f93618c2019-01-21WarningsExact identifier
spl id: f5322af7-72d0-430a-a3b3-6fd09c2f088a
spl set id: 943e9f7f-ec0e-483a-9171-0cd64f93618c

Reported adverse events (FAERS/openFDA)#

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