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GUNA-MELATONIN - 17089-458-18 - (MELATONIN)

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Drug Information of GUNA-MELATONIN

Product NDC: 17089-458
Proprietary Name: GUNA-MELATONIN
Non Proprietary Name: MELATONIN
Active Ingredient(s): 4    [hp_C]/30mL & nbsp;   MELATONIN
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-MELATONIN

Product NDC: 17089-458
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110523

Package Information of GUNA-MELATONIN

Package NDC: 17089-458-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-458-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-MELATONIN

NDC Code 17089-458-18
Proprietary Name GUNA-MELATONIN
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-458-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MELATONIN
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20110523
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name MELATONIN
Strength Number 4
Strength Unit [hp_C]/30mL
Pharmaceutical Classes

Complete Information of GUNA-MELATONIN


General Information