NDC 15631-0385

SALIX NIGRA

Salix Nigra

SALIX NIGRA 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 Salix Nigra Bark.

Product ID15631-0385_a1bf5aa5-4f90-ae04-e053-2a95a90afb49
NDC15631-0385
Product TypeHuman Otc Drug
Proprietary NameSALIX NIGRA
Generic NameSalix Nigra
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSALIX NIGRA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0385-0

100 PELLET in 1 PACKAGE (15631-0385-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0385-0 [15631038500]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0385-1 [15631038501]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0385-4 [15631038504]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0385-5 [15631038505]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0385-3 [15631038503]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0385-2 [15631038502]

SALIX NIGRA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
SALIX NIGRA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:f1cbea47-adaa-441e-8927-e31dce78e82a
Manufacturer
UNII

NDC Crossover Matching brand name "SALIX NIGRA" or generic name "Salix Nigra"

NDCBrand NameGeneric Name
15631-0385SALIX NIGRASALIX NIGRA
15631-0678SALIX NIGRASALIX NIGRA
68428-616Salix nigraSALIX NIGRA BARK
71919-603Salix nigraSALIX NIGRA BARK
22840-4416Black Willow PollenSalix nigra
22840-4491Black Willow PollenSalix nigra
22840-5478Black Willow PollenSalix nigra
49643-409Black Willow PollenSalix nigra

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