Precaine B Chocolate Vanilla

Product NDC
10866-0089
11-digit product format
108660089
Labeler code
10866
Product ID
10866-0089_9cc0c4ef-0922-e067-e053-2a95a90a321c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benzocaine Topical Anesthetic
Dosage form
GEL
Route
DENTAL
Labeler
Pascal Company, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-08-16
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
221 mg/g
Pharmacologic classes
Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
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
10866-0089-12022-01-28C16284748780-1d6a99b39-ba6d-a426-e053-dadaa90af4c2Precaine B Chocolate Vanilla

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10866-0089-1Precaine B Chocolate Vanilla30 g in 1 JARGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10866-0089PRECAINE B CHOCOLATE VANILLA (BENZOCAINE TOPICAL ANESTHETIC) GEL [PASCAL COMPANY, INC.]2Legacy NDC, 1 package rows20200123_5c630601-5060-1d77-e053-2a91aa0a00b7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10866-0089-11086600890130 g in 1 JAR (10866-0089-1) 30 g2017-08-160000-00-00NoNoCurrent