SNAIL REPAIR BLEMISH BALM

Manufacturer
Coson Co., Ltd.
Effective date
2014-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:39:00

Label at a glance#

ProductSNAIL REPAIR BLEMISH BALM
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Indications and uses

Indication and Usage: In the last step of skin care, spread and tap it softly on the whole face.

Dosage and administration

Dosage and Administration: For your face, use it about same amout as a size of been(about 1.5mL)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:
ETHYLHEXYL METHOXYCINNAMATE 5.65%, TITANIUM DIOXIDE 8,98%, ZINC OXIDE 0.7656%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
SNAIL SECRETION FILTRATE, CYCLOPENTASILOXANE, POLYMETHYL METHACRYLATE, PEG/PPG-17/6 COPOLYMER, DICAPRYLYL CARBONATE, DIMETHICONE, CETYL PEG/PPG-10/1 DIMETHICONE, ARBUTINE, SODIUMCHLORIDE, OZOKERITE, CYCLOPENTASILOXANE, TRIETHYL CITRATE,DISTEARDIMONIUM HECTORITE,GLYCOSYLTREHALOSE,HYDROGENATED STARCH HYDROLYSATE,CALCIUM STEARATE,HEXYL LAURATE, SORBITAN SESQUIOLEATE,SODIUM HYALURONATE,LAURYLPEG/PPG-18/18 METHICONE,SORBITAN SESQUIOLEATE,ALLANTOIN,PANTHENOL,BETA-GLUCAN,ADENOSINE,LECITHIN,TOCOPHERYL ACETATE ,CAPRYLIC/CAPRIC TRIGLYCERIDE,UBIQUINONE ,DIISOPROPYL ADIPATE,GLYCERIN,ARNICA MONTANA FLOWER EXTRACT,ARTEMISIA ABSINTHIUM EXTRACT,ACHILLEA MILLEFOLIUM EXTRACT ,GENTIANA LUTEA ROOT EXTRACT ,ETHANOL,CASTANEA SATIVA(CHESTNUT) SEED EXTRACT,CARICA PAPAYA(PAPAYA) FRUIT EXTRACT,LAVANDULA ANGUSTIFOLIA(LAVENDER)EXTRACT,CORNUSOFFICINALIS FRUIT EXTRACT,CAPRYLYL GLYCOL,ETHYLHEXYLGLYCERIN,TROPOLONE,DISODIUM EDTA,FRAGRANCE,CI 77491 ,CI 77492 ,CI 77499

PURPOSE

OTC - PURPOSE SECTION

Purpose: UVA/UVB Protection

WARNINGS

WARNINGS SECTION

Warnings:
1. If following symptoms occur, stop use and consult a doctor : red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight.
2. Do not use on scarred skin, or if you have dermatitis or eczema
3. Keep the cap close on its product
4. Keep away from direct sunlight or heat.
5. This product blocks UVA rays and ultraviolet protection effectiveness have been measured by the Food and Drug Administration methods and standards

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 AND USAGE

INDICATIONS & USAGE SECTION

Indication and Usage:
In the last step of skin care, spread and tap it softly on the whole face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and Administration:
For your face, use it about same amout as a size of been(about 1.5mL)

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
62171-030-012020-01-31C16284748780-19d75b9d0-a864-f424-e053-dadaa90a57ce9025aecb-a806-41d5-9052-408acdb699ec

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62171-030-01SNAIL REPAIR BLEMISH BALM50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62171-030SNAIL REPAIR BLEMISH BALM (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [COSON CO., LTD.]1Legacy NDC, 1 package rows20140417_9025aecb-a806-41d5-9052-408acdb699ec.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
TRIETHYL CITRATEINACTIVE INGREDIENT8Z96QXD6UM1

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
62171-03062171-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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 · 19 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, FILM COATED, EXTENDED RELEASE / ORAL1 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, ORALLY DISINTEGRATING / ORAL17 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, EXTENDED RELEASE / ORAL160 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, DELAYED RELEASE / ORAL70 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, COATED, EXTENDED RELEASE / ORAL7 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, COATED PELLETS / ORAL147 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL100 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, EXTENDED RELEASE / ORAL129 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, CHEWABLE / ORAL34 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMGRANULE, FOR SUSPENSION / ORAL64 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, COATED / ORAL7 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET / ORAL52 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMSUSPENSION / ORAL71 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMINJECTION, POWDER, FOR SUSPENSION / INTRAMUSCULAR10 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE, DELAYED RELEASE PELLETS / ORAL147 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMCAPSULE / ORAL10 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, FILM COATED / ORAL3 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMTABLET, DELAYED RELEASE / ORAL120 mgExact identifier — unii candidate
19 equally ranked IID candidates
TRIETHYL CITRATETRIETHYL CITRATE8Z96QXD6UMSUSPENSION, EXTENDED RELEASE / ORAL5 mgExact identifier — unii candidate
19 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
3fc805e4-186d-4186-9697-f978aa8e0fff9025aecb-a806-41d5-9052-408acdb699ec2014-04-17WarningsExact identifier
spl id: 3fc805e4-186d-4186-9697-f978aa8e0fff
spl set id: 9025aecb-a806-41d5-9052-408acdb699ec

Reported adverse events (FAERS/openFDA)#

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