FDA.reportPublic FDA data

DABIDA EXTREME SKIN TAG REMOVER

Manufacturer
Natural Korea Co., Ltd.
Effective date
2020-10-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:27

Label at a glance#

ProductDABIDA EXTREME SKIN TAG REMOVER
Active ingredientTHUJA OCCIDENTALIS LEAF
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ABIDA EXTREME SKIN TAG REMOVERABIDA EXTREME SKIN TAG REMOVER

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X002KUZIIDDABIDA.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74646-0016-12023-01-30C16284748780-1f386c649-f751-0266-e053-dadaa90a7c1a[OTC-HOMEOPHATIC] DABIDA EXTREME SKIN TAG REMOVER: 74646-0016-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74646-0016-1DABIDA EXTREME SKIN TAG REMOVER1 in 1 BOXCREAM11
74646-0016-1DABIDA EXTREME SKIN TAG REMOVER15 mL in 1 TUBE, WITH APPLICATORCREAM151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74646-0016DABIDA EXTREME SKIN TAG REMOVER (THUJA OCCIDENTALIS) CREAM [NATURAL KOREA CO., LTD.]1Legacy NDC, 2 package rows20201027_b2a18fac-6b74-2ff4-e053-2995a90aff7b.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74646-001674646-0016-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 806OZP39ZG8HIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ARGAN OIL4V59G5UW9XIACT
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
GLUCONOLACTONEWQ29KQ9POTIACT
GLYCERINPDC6A3C0OXIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
WATER059QF0KO0RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
CETYL ALCOHOL936JST6JCNIACT
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
CETYL ETHYLHEXANOATE134647WMX4IACT
PULSATILLA KOREANA WHOLE5R35881OBKIACT
ISOHEXADECANE918X1OUF1EIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
STEARIC ACID4ELV7Z65APIACT
CENTELLA ASIATICA7M867G6T1UIACT
MADECASSOSIDECQ2F5O6YIYIACT
SUNFLOWER OIL3W1JG795YIIACT
ZANTHOXYLUM PIPERITUM FRUIT PULP7PFC2VA251IACT
GRAPEFRUITO82C39RR8CIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
SALICYLIC ACIDO414PZ4LPZIACT
TEA TREE OILVIF565UC2GIACT
ALLANTOIN344S277G0ZIACT

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
b2a18fbb-95f6-a196-e053-2a95a90a6a5cb2a18fac-6b74-2ff4-e053-2995a90aff7b2020-10-27Exact identifier
spl id: b2a18fbb-95f6-a196-e053-2a95a90a6a5c
spl set id: b2a18fac-6b74-2ff4-e053-2995a90aff7b

Reported adverse events (FAERS/openFDA)#

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