FDA.reportPublic FDA data

Tag Away

Manufacturer
Pure Source
Effective date
2012-09-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:04:03

Label at a glance#

ProductTag Away
Active ingredientTHUJA OCCIDENTALIS WHOLE
Label structure8 sections

Dosage and administration

Use cotton swab to apply 3 times daily to affected area. Skin tags will dry and flake away over a 3-8 week period. Skin test for tolerability. If irritation occurs, discontinue use.

Label contents#

Full prescribing information#

Warnings:

WARNINGS SECTION

For external use only. If pregnant, or breast feeding, ask a health care professional before use. Avoid using near eyes. If swallowed, get medical help or contact poison control hotline immediately at 800-222-1222.

Directions:

DOSAGE & ADMINISTRATION SECTION

Use cotton swab to apply 3 times daily to affected area. Skin tags will dry and flake away over a 3-8 week period. Skin test for tolerability. If irritation occurs, discontinue use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

cedar leaf oil, melaleuca alternifolia leaf oil, ricinus communis seed oil

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X HPUS

The letters HPUS indicate the components(s) in this product is (are) offically monographed in the Homeopathic Pharmacopeia of the United States

Purpose:

OTC - PURPOSE SECTION

Polypi, Naevi, Skin Tubercles Symptom Relief.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions:

INDICATIONS & USAGE SECTION

Use cotton swab to apply 3 times daily to affected area. Skin tags will dry and flake away over a 3-8 week period. Skin test for tolerability. If irritation occurs, discontinue use.

TagAway 15 oz.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65121-623-152019-11-27C16284748780-19855d018-dd03-cd31-e053-dbdaa90ab51aTag Away 15 ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65121-623-15Tag Away15 mL in 1 PACKAGELIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65121-623TAG AWAY (THUJA OCCIDENTALIS) LIQUID [PURE SOURCE]1Legacy NDC, 1 package rows20121015_ac7656d1-eb7a-44fd-ad3c-f03fbd93b820.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
THUJA OCCIDENTALIS WHOLEACTIVE INGREDIENT5HBV6WCE3N1
THUJA OCCIDENTALIS WHOLEACTIVE MOIETY5HBV6WCE3N1
CEDAR LEAF OILINACTIVE INGREDIENTBJ169U4NLG1
MELALEUCA ALTERNIFOLIA LEAFINACTIVE INGREDIENTG43C57162K1
RICINUS COMMUNIS SEEDINACTIVE INGREDIENT7EK4SFN1TX1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65121-62365121-623-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
THUJA OCCIDENTALIS WHOLE5HBV6WCE3NACTIM
CEDAR LEAF OILBJ169U4NLGIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
RICINUS COMMUNIS SEED7EK4SFN1TXIACT

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
1c691b70-50c9-438e-ae19-ee9372ae690eac7656d1-eb7a-44fd-ad3c-f03fbd93b8202012-09-06WarningsExact identifier
spl id: 1c691b70-50c9-438e-ae19-ee9372ae690e
spl set id: ac7656d1-eb7a-44fd-ad3c-f03fbd93b820

Reported adverse events (FAERS/openFDA)#

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