Noble G Plus

Product NDC
60319-3001
11-digit product format
603193001
Labeler code
60319
Product ID
60319-3001_990201fb-aea2-cf20-e053-2995a90a1ace
Type
HUMAN OTC DRUG
Nonproprietary name
XYLITOL
Dosage form
PASTE, DENTIFRICE
Route
DENTAL
Labeler
Hankuk Bowonbio Co., Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-11-30
Marketing end
0000-00-00
Substance
XYLITOL
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct60319-3001IInactivated by FDA2026-08-10
excluded packagepackage60319-300160319-3001-1IInactivated by FDA2026-08-10

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductIInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage60319-3001-1IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductIInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage60319-3001-1IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproductIInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage60319-3001-1IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproductIInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage60319-3001-1IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductIInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage60319-3001-1IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductIInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage60319-3001-1IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproductUExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage60319-3001-1UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproductUExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage60319-3001-1UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproductUExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage60319-3001-1UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60319-3001-12025-01-30C16284748780-12cef2736-60fa-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60319-3001-1Noble G Plus130 g in 1 TUBEPASTE, DENTIFRICE1302

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
XYLITOLACTIVE INGREDIENTVCQ006KQ1ENOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
XYLITOLACTIVE MOIETYVCQ006KQ1ENOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
CHITOSAN OLIGOSACCHARIDEINACTIVE INGREDIENT23R93M6Y64NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
GOLDINACTIVE INGREDIENT79Y1949PYONOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
GREEN TEA LEAFINACTIVE INGREDIENTW2ZU1RY8B0NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
HYDRATED SILICAINACTIVE INGREDIENTY6O7T4G8P9NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
ISOSTEARIC ACIDINACTIVE INGREDIENTX33R8U0062NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
LEVOMENTHOLINACTIVE INGREDIENTBZ1R15MTK7NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
POLYETHYLENE GLYCOL 1500INACTIVE INGREDIENT1212Z7S33ANOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HNOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
SACCHARIN SODIUM ANHYDROUSINACTIVE INGREDIENTI4807BK602NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JNOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
SODIUM MONOFLUOROPHOSPHATEINACTIVE INGREDIENTC810JCZ56QNOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
SORBITOLINACTIVE INGREDIENT506T60A25RNOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
TRIBASIC CALCIUM PHOSPHATEINACTIVE INGREDIENT91D9GV0Z28NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1
WATERINACTIVE INGREDIENT059QF0KO0RNOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60319-3001NOBLE G PLUS (XYLITOL) PASTE, DENTIFRICE [HANKUK BOWONBIO CO., LTD]2Legacy NDC, 1 package rows20191206_0392a152-ee0d-4f9d-a85f-02170473d6eb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60319-3001-160319300101130 g in 1 TUBE (60319-3001-1) 130 g2019-12-060000-00-00NoNoCurrent