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Hangover Relief - 61727-330-21 - (ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.)

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Drug Information of Hangover Relief

Product NDC: 61727-330
Proprietary Name: Hangover Relief
Non Proprietary Name: ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.
Active Ingredient(s): 5; 5; 5; 5; 5; 7; 5; 5; 5    [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g & nbsp;   ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hangover Relief

Product NDC: 61727-330
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20111123

Package Information of Hangover Relief

Package NDC: 61727-330-21
Package Description: 4 g in 1 TUBE (61727-330-21)

NDC Information of Hangover Relief

NDC Code 61727-330-21
Proprietary Name Hangover Relief
Package Description 4 g in 1 TUBE (61727-330-21)
Product NDC 61727-330
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20111123
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name ASAFETIDA; CAPSICUM; COLA NUT; LACHESIS MUTA VENOM; POTASSIUM DICHROMATE; RANUNCULUS BULBOSUS; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; ZINC
Strength Number 5; 5; 5; 5; 5; 7; 5; 5; 5
Strength Unit [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g
Pharmaceutical Classes

Complete Information of Hangover Relief


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