eQo Gel

Product NDC
79838-002
11-digit product format
798380002
Labeler code
79838
Product ID
79838-002_af5dc601-72b2-ea45-e053-2a95a90a2bb0
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
INTERNATIONAL HARBOR LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79838-002-01eQo Gel3785 mL in 1 BOTTLEGEL37852
79838-002-02eQo Gel250 mL in 1 BOTTLEGEL2502
79838-002-03eQo Gel500 mL in 1 BOTTLEGEL5002
79838-002-04eQo Gel1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79838-002EQO GEL (ALCOHOL) GEL [INTERNATIONAL HARBOR LLC]2Legacy NDC, 4 package rows20200916_adbb2029-c51e-2384-e053-2995a90af28d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79838-002-01798380002013785 mL in 1 BOTTLE (79838-002-01) 3785 ml2020-03-300000-00-00NoNoCurrent
79838-002-0279838000202250 mL in 1 BOTTLE (79838-002-02) 250 ml2020-03-300000-00-00NoNoCurrent
79838-002-0379838000203500 mL in 1 BOTTLE (79838-002-03) 500 ml2020-03-300000-00-00NoNoCurrent
79838-002-04798380002041000 mL in 1 BOTTLE (79838-002-04) 1000 ml2020-03-300000-00-00NoNoCurrent