TONYMOLY INTENSE CARE SNAIL BB

Manufacturer
Tonymoly Co., Ltd. | Cosmecca Korea Co.,Ltd.
Effective date
2015-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:52

Label at a glance#

ProductTONYMOLY INTENSE CARE SNAIL BB
Active ingredientTitanium Dioxide, Zinc Oxide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium Dioxide 9.01%, Zinc Oxide 6.30%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Snail Secretion Filtrate, Butylene Glycol, Phenyl Trimethicone, Dimethicone, Dipentaerythrityl Hexahydroxystearate/Hexastearate/Hexarosinate, Butylene Glycol Dicaprylate/Dicaprate, Orbignya Oleifera Seed Oil, Cetyl PEG/PPG-10/1 Dimethicone, Arbutin, Magnesium Sulfate, Aluminum Hydroxide, Stearic Acid, Iron Oxides (CI 77492), Water, Caprylyl Glycol, Polyglyceryl-4 Isostearate, Hexyl Laurate, Triethoxycaprylylsilane, Phenoxyethanol, Ethylhexylglycerin, Dimethicone/Vinyl Dimethicone Crosspolymer, Talc, Iron Oxides (CI 77499), Iron Oxides (CI 77491), Tocopheryl Acetate, Sorbitan Isostearate, Rosa Canina Fruit Oil, Calcium Stearate, 1,2-Hexanediol, Glycerin, Imperata Cylindrica Root Extract, Adenosine, Disodium EDTA, Citrus Medica Limonum (Lemon) Peel Oil, Camellia Sinensis Callus Culture Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Oryza Sativa (Rice) Callus Culture Extract, Leontopodium Alpinum Callus Culture Extract, PEG-8, Citrus aurantium dulcis (orange) peel oil, Steareth-20, Citrus Aurantifolia (Lime) Oil, Pinus Sylvestris Leaf Oil, Eucalyptus Globulus Leaf Oil, Centella Asiatica Extract, Carbomer, Aloe Barbadensis Leaf Juice, Usnea Barbata (Lichen) Extract, Zanthoxylum Piperitum Fruit Extract, Xanthan Gum, Pulsatilla Koreana Extract, N-Hydroxysuccinimide, Potassium sorbate, Sodium Hyaluronate, Lecithin, Sodium Benzoate, Acetyl Hexapeptide-8, Palmitoyl Oligopeptide, Chrysin, Palmitoyl Tetrapeptide-7, Chlorhexidine digluconate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warning: 1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children: Keep out of reach of babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indication & Usage: After application of skin care products, apply on face using fingers or sponge.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of cartonImage of carton

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
59078-051-012025-11-09C16284748780-19d75b9d0-de0a-f424-e053-dadaa90a57ce5019abfb-9f92-4360-ab0d-42a6d766c23f
59078-051-012020-01-31C16284748780-19d75b9d0-de0a-f424-e053-dadaa90a57ce5019abfb-9f92-4360-ab0d-42a6d766c23f

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59078-051TONYMOLY INTENSE CARE SNAIL BB (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [TONYMOLY CO., LTD.]1Legacy NDC20150303_5019abfb-9f92-4360-ab0d-42a6d766c23f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
Phenyl TrimethiconeINACTIVE INGREDIENTDR0K5NOJ4R1

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
59078-05159078-051-01

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

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
43297750-ae0f-0876-e063-6394a90a354d5019abfb-9f92-4360-ab0d-42a6d766c23f2025-11-09WarningsExact identifier
spl set id: 5019abfb-9f92-4360-ab0d-42a6d766c23f

Reported adverse events (FAERS/openFDA)#

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