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Motion Sickness - 54973-9147-1 - (STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE, and ANAMIRTA COCCULUS SEED)

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Drug Information of Motion Sickness

Product NDC: 54973-9147
Proprietary Name: Motion Sickness
Non Proprietary Name: STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE, and ANAMIRTA COCCULUS SEED
Active Ingredient(s): 30; 12; 6; 6    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE, and ANAMIRTA COCCULUS SEED
Administration Route(s): ORAL
Dosage Form(s): TABLET, SOLUBLE
Coding System: National Drug Codes(NDC)

Labeler Information of Motion Sickness

Product NDC: 54973-9147
Labeler Name: Hyland's
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19941201

Package Information of Motion Sickness

Package NDC: 54973-9147-1
Package Description: 50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9147-1)

NDC Information of Motion Sickness

NDC Code 54973-9147-1
Proprietary Name Motion Sickness
Package Description 50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9147-1)
Product NDC 54973-9147
Product Type Name HUMAN OTC DRUG
Non Proprietary Name STRYCHNOS NUX-VOMICA SEED, TOBACCO LEAF, KEROSENE, and ANAMIRTA COCCULUS SEED
Dosage Form Name TABLET, SOLUBLE
Route Name ORAL
Start Marketing Date 19941201
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Hyland's
Substance Name ANAMIRTA COCCULUS SEED; KEROSENE; STRYCHNOS NUX-VOMICA SEED; TOBACCO LEAF
Strength Number 30; 12; 6; 6
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Motion Sickness


General Information