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Neti Wash Flu - 61727-401-30 - (HAEMOPHILUS INFLUENZAE TYPE B)

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Drug Information of Neti Wash Flu

Product NDC: 61727-401
Proprietary Name: Neti Wash Flu
Non Proprietary Name: HAEMOPHILUS INFLUENZAE TYPE B
Active Ingredient(s): 9    [hp_C]/29.5mL & nbsp;   HAEMOPHILUS INFLUENZAE TYPE B
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Neti Wash Flu

Product NDC: 61727-401
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20120105

Package Information of Neti Wash Flu

Package NDC: 61727-401-30
Package Description: 29.5 mL in 1 BOTTLE, DROPPER (61727-401-30)

NDC Information of Neti Wash Flu

NDC Code 61727-401-30
Proprietary Name Neti Wash Flu
Package Description 29.5 mL in 1 BOTTLE, DROPPER (61727-401-30)
Product NDC 61727-401
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HAEMOPHILUS INFLUENZAE TYPE B
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20120105
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name HAEMOPHILUS INFLUENZAE TYPE B
Strength Number 9
Strength Unit [hp_C]/29.5mL
Pharmaceutical Classes

Complete Information of Neti Wash Flu


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