anal GLIDE

Product NDC
70742-092
11-digit product format
707420092
Labeler code
70742
Product ID
70742-092_bd0dd8a9-3d50-4b11-bed0-28e5efc99fb7
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOCAINE
Dosage form
GEL
Route
TOPICAL
Labeler
Product Max Group Inc
Application
part348
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-06-15
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
2833 mg/60mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70742-092-012020-01-31C16284748780-19d75b9cf-f4c1-f424-e053-dadaa90a57ceanal GLIDE - 092

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70742-092-01anal GLIDE60 mL in 1 BOTTLE, PUMPGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70742-092ANAL GLIDE (BENZOCAINE) GEL [PRODUCT MAX GROUP INC]1Legacy NDC, 1 package rows20160808_55ac41c4-c0ff-4846-9a6f-39aedbe7d545.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70742-092-017074200920160 mL in 1 BOTTLE, PUMP60 mlHistorical