Skin Tag Relief

Product NDC
68229-100
11-digit product format
682290100
Labeler code
68229
Product ID
68229-100_262e23fb-5ad8-bbde-e063-6394a90ab37b
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja Occidentalis Leafy Twig
Dosage form
OIL
Route
TOPICAL
Labeler
Quest Products, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-05-21
Substance
THUJA OCCIDENTALIS LEAFY TWIG
Active strength
6 [hp_X]/10mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Skin Tag Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/10mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1NT28V9397Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
98fb9d4a-d0d2-425b-878b-927eebf53067Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68229-100-022020-02-03C16284748780-19d75b9cf-fd88-f424-e053-dadaa90a57ceSkin Tag Relief
68229-100-022020-01-31C16284748780-19d75b9cf-fd88-f424-e053-dadaa90a57ceSkin Tag Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68229-100-01Skin Tag Relief10 mL in 1 BOTTLE, WITH APPLICATOROIL107
68229-100-02Skin Tag Relief1 in 1 CARTONOIL17
68229-100-03Skin Tag Relief12.5 mL in 1 BOTTLE, WITH APPLICATOROIL12.57
68229-100-04Skin Tag Relief1 in 1 CARTONOIL17

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68229-100SKIN TAG RELIEF (THUJA OCCIDENTALIS LEAFY TWIG) OIL [QUEST PRODUCTS, INC.]7Current NDC, Legacy NDC, 4 package rows20241107_98fb9d4a-d0d2-425b-878b-927eebf53067.zip

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
Skin Tag ReliefTHUJA OCCIDENTALIS LEAFY TWIGQuest Products, Inc.98fb9d4a-d0d2-425b-878b-927eebf530672024-11-05WarningsExact identifier
ndc (product): 68229-100

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68229-100-016822901000110 mL in 1 BOTTLE, WITH APPLICATOR10 mlHistorical
68229-100-02682290100021 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) / 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01) 2013-05-210000-00-00NoNoCurrent
68229-100-036822901000312.5 mL in 1 BOTTLE, WITH APPLICATOR12.5 mlHistorical
68229-100-04682290100041 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-04) / 12.5 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-03) 2022-05-230000-00-00NoNoCurrent