DR FROG PP SUN BLOCK

Manufacturer
Charmzone Co Ltd | Charmzone Co., Ltd._Wonju Factory
Effective date
2018-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:12

Label at a glance#

ProductDR FROG PP SUN BLOCK
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: TITANIUM DIOXIDE 7.30%, ZINC OXIDE 6.99%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

WATER,CYCLOPENTASILOXANE,ANGELICA ARCHANGELICA ROOT WATER,BUTYLENE GLYCOL,CYCLOMETHICONE,ISODODECANE,HYDROGENATED POLY(C6-14 OLEFIN),PEG-10 DIMETHICONE, PHENYL TRIMETHICONE,DIMETHICONE,1,2-HEXANEDIOL,DISTEARDIMONIUM HECTORITE,PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE,ALUMINUM HYDROXIDE,SODIUM CHLORIDE,STEARIC ACID,CYCLOHEXASILOXANE,DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER,BEESWAX,GLYCERIN,GLYCERYL CAPRYLATE,FRAGRANCE,MYRISTIC ACID,TOCOPHERYL ACETATE,CETYL PEG/PPG-10/1 DIMETHICONE,SACCHAROMYCES/RUBUS COREANUS FRUIT FERMENT FILTRATE,HYACINTHUS ORIENTALIS (HYACINTH) EXTRACT,ALLIUM CEPA (ONION) BULB EXTRACT,CENTELLA ASIATICA EXTRACT,HIPPOPHAE RHAMNOIDES FRUIT EXTRACT,PANTHENOL,PROPYLENE GLYCOL,ETHYLHEXYLGLYCERIN,DIOSPYROS KAKI LEAF EXTRACT,MICA,DISODIUM EDTA,IRON OXIDES(CI 77491),GLYCERETH-26,BETAINE,CAPRYLIC/CAPRIC TRIGLYCERIDE,DIPROPYLENE GLYCOL,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL,TRIETHOXYCAPRYLYLSILANE,RAFFINOSE,HYDROGENATED LECITHIN,HIPPOPHAE RHAMNOIDES EXTRACT,ASCORBYL TOCOPHERYL ACETATE,SODIUM GUAIAZULENE SULFONATE,SODIUM HYALURONATE,SUCROSE PALMITATE,ALCOHOL,POLYSORBATE 80,CERAMIDE NP,NELUMBO NUCIFERA LEAF EXTRACT,CHOLESTEROL,GLYCINE,GLUTAMINE,ASPARAGINE,PHYTOSPHINGOSINE

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

1) Please stop using the product if the following symptoms occur or appear when the skin is exposed to direct sunlight: red blotches, swelling, itchiness or other irritations while using product. Then, consult a dermatologist or a specialist.

2) Please do not apply the product on wound or any of skin irritation, such as eczema or dermatitis.

3) Precaution during storage/handling. a) Keep the product closed after using b) Keep out of reach of children c) Avoid storing in high and low temperature and areas exposed to direct sunlight

DESCRIPTION

DESCRIPTION SECTION

Uses:

[UV PROTECTION]

SPF50+/PA++++

Sun block of Intensive UV defense along with natural toning up, enabling pink-shining and glossy skin.

1. Intensified UVA/UVB defense Intensified UV filter of SPF50+/PA++++ keeps skin healthy by further screening the UV rays.

2. Correct skin tone and texture Keeps the tone natural and lively, at the same time the pink aura tidies up the skin texture glossy.

3. Moisturization formula of less irritation Nature-derived ingredients such as angelica root, hyacinth, and sea buckthorn extracts keep skin moisty and lively from dryness caused by UV rays.

Directions:

Take an appropriate amount and apply to the entire face along with your neck, especially to parts of which can be vulnerable to UV rays at the end of skin care routine or right before the point putting on the make-up.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
22201-1040-22020-01-31C16284748780-19d75b9d0-7e3a-f424-e053-dadaa90a57ce71206697-924c-43a4-9d11-1d14520e5192

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
22201-1040-1DR FROG PP SUN BLOCK50 mL in 1 TUBECREAM501
22201-1040-2DR FROG PP SUN BLOCK1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
22201-1040DR FROG PP SUN BLOCK (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [CHARMZONE CO LTD]1Legacy NDC, 2 package rows20180413_71206697-924c-43a4-9d11-1d14520e5192.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22201-104022201-1040-1, 22201-1040-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
243ca685-56a5-4fd5-8476-e597b17aa7ea71206697-924c-43a4-9d11-1d14520e51922018-04-13WarningsExact identifier
spl id: 243ca685-56a5-4fd5-8476-e597b17aa7ea
spl set id: 71206697-924c-43a4-9d11-1d14520e5192

Reported adverse events (FAERS/openFDA)#

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