GUNA-EGF - 17089-372-18 - (EPIDERMAL GROWTH FACTOR)

Alphabetical Index


Drug Information of GUNA-EGF

Product NDC: 17089-372
Proprietary Name: GUNA-EGF
Non Proprietary Name: EPIDERMAL GROWTH FACTOR
Active Ingredient(s): 4    [hp_C]/30mL & nbsp;   EPIDERMAL GROWTH FACTOR
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-EGF

Product NDC: 17089-372
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110331

Package Information of GUNA-EGF

Package NDC: 17089-372-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-372-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-EGF

NDC Code 17089-372-18
Proprietary Name GUNA-EGF
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-372-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-372
Product Type Name HUMAN OTC DRUG
Non Proprietary Name EPIDERMAL GROWTH FACTOR
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20110331
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name HUMAN EPIDERMAL GROWTH FACTOR
Strength Number 4
Strength Unit [hp_C]/30mL
Pharmaceutical Classes

Complete Information of GUNA-EGF


General Information