NDC 15631-0386

SALVIA OFFICINALIS

Salvia Officinalis

SALVIA OFFICINALIS 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 Sage.

Product ID15631-0386_09e8f68d-90ea-4d78-aa49-12759bca7768
NDC15631-0386
Product TypeHuman Otc Drug
Proprietary NameSALVIA OFFICINALIS
Generic NameSalvia Officinalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSAGE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0386-0

100 PELLET in 1 PACKAGE (15631-0386-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0386-4 [15631038604]

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

NDC 15631-0386-0 [15631038600]

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

NDC 15631-0386-2 [15631038602]

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

NDC 15631-0386-1 [15631038601]

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

NDC 15631-0386-3 [15631038603]

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

NDC 15631-0386-5 [15631038605]

SALVIA OFFICINALIS 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
SAGE1 [hp_X]/1

OpenFDA Data

SPL SET ID:7984ce40-29d4-44fc-93e6-491fcd32a6fd
Manufacturer
UNII

NDC Crossover Matching brand name "SALVIA OFFICINALIS" or generic name "Salvia Officinalis"

NDCBrand NameGeneric Name
15631-0386SALVIA OFFICINALISSALVIA OFFICINALIS
37662-1192Salvia OfficinalisSalvia Officinalis
37662-1193Salvia OfficinalisSalvia Officinalis
37662-1194Salvia OfficinalisSalvia Officinalis
37662-1195Salvia OfficinalisSalvia Officinalis
37662-1196Salvia OfficinalisSalvia Officinalis
37662-1197Salvia OfficinalisSalvia Officinalis
37662-1198Salvia OfficinalisSalvia Officinalis
37662-1199Salvia OfficinalisSalvia Officinalis
68428-617Salvia officinalisSAGE
71919-604Salvia officinalisSAGE

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