NDC 15631-0239

IRIS TENAX

Iris Tenax

IRIS TENAX is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Iris Tenax.

Product ID15631-0239_4010a564-4526-4082-9efb-dc334b67e2de
NDC15631-0239
Product TypeHuman Otc Drug
Proprietary NameIRIS TENAX
Generic NameIris Tenax
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameIRIS TENAX
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0239-0

100 PELLET in 1 PACKAGE (15631-0239-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0239-3 [15631023903]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0239-0 [15631023900]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0239-1 [15631023901]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0239-5 [15631023905]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0239-2 [15631023902]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0239-4 [15631023904]

IRIS TENAX PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
IRIS TENAX1 [hp_X]/1

OpenFDA Data

SPL SET ID:0d80118f-3c5d-48af-b63b-8a40ee68f14d
Manufacturer
UNII

NDC Crossover Matching brand name "IRIS TENAX" or generic name "Iris Tenax"

NDCBrand NameGeneric Name
0220-2688Iris tenaxIRIS TENAX
15631-0239IRIS TENAXIRIS TENAX
68428-960Iris tenaxIRIS TENAX
71919-368Iris tenaxIRIS TENAX

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