Benzoin Tincture

Product NDC
0395-9107
11-digit product format
003959107
Labeler code
0395
Product ID
0395-9107_a878b139-8995-e154-e053-2995a90a621e
Type
HUMAN OTC DRUG
Nonproprietary name
Benzoin Resin
Dosage form
LIQUID
Route
TOPICAL
Labeler
Humco Holding Group, Inc.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2008-01-01
Marketing end
0000-00-00
Substance
BENZOIN RESIN
Active strength
1000 mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0395-9107-922022-07-29C16284748780-1e4f33bdf-b0b1-d8a0-e053-dadaa90a6e4ePrivate Label Benzoin Tincture

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0395-9107-92Benzoin Tincture59 mL in 1 BOTTLE, PLASTICLIQUID593

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0395-9107BENZOIN TINCTURE (BENZOIN RESIN) LIQUID [HUMCO HOLDING GROUP, INC.]3Legacy NDC, 1 package rows20200620_60517f09-674c-ea0c-e053-2991aa0a9b92.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0395-9107-920039591079259 mL in 1 BOTTLE, PLASTIC (0395-9107-92) 59 ml2017-12-120000-00-00NoNoCurrent