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Morning Sickness - 50845-0100-1 - (Symphoricarpus racemosus,)

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Drug Information of Morning Sickness

Product NDC: 50845-0100
Proprietary Name: Morning Sickness
Non Proprietary Name: Symphoricarpus racemosus,
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   Symphoricarpus racemosus,
Administration Route(s): ORAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Morning Sickness

Product NDC: 50845-0100
Labeler Name: Liddell Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110524

Package Information of Morning Sickness

Package NDC: 50845-0100-1
Package Description: 30 mL in 1 BOTTLE, SPRAY (50845-0100-1)

NDC Information of Morning Sickness

NDC Code 50845-0100-1
Proprietary Name Morning Sickness
Package Description 30 mL in 1 BOTTLE, SPRAY (50845-0100-1)
Product NDC 50845-0100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Symphoricarpus racemosus,
Dosage Form Name SPRAY
Route Name ORAL
Start Marketing Date 20110524
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Liddell Laboratories, Inc.
Substance Name SYMPHORICARPOS ALBUS FRUIT
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of Morning Sickness


General Information