GUNA-IL 3 - 17089-381-18 - (INTERLEUKIN-3)

Alphabetical Index


Drug Information of GUNA-IL 3

Product NDC: 17089-381
Proprietary Name: GUNA-IL 3
Non Proprietary Name: INTERLEUKIN-3
Active Ingredient(s): 4    [hp_C]/30mL & nbsp;   INTERLEUKIN-3
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-IL 3

Product NDC: 17089-381
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20080617

Package Information of GUNA-IL 3

Package NDC: 17089-381-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-381-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-IL 3

NDC Code 17089-381-18
Proprietary Name GUNA-IL 3
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-381-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-381
Product Type Name HUMAN OTC DRUG
Non Proprietary Name INTERLEUKIN-3
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20080617
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name INTERLEUKIN-3
Strength Number 4
Strength Unit [hp_C]/30mL
Pharmaceutical Classes

Complete Information of GUNA-IL 3


General Information