NDC 15631-0311

NATRUM SALICYLICUM

Natrum Salicylicum

NATRUM SALICYLICUM 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 Sodium Salicylate.

Product ID15631-0311_a199c240-f639-5db2-e053-2995a90af7dc
NDC15631-0311
Product TypeHuman Otc Drug
Proprietary NameNATRUM SALICYLICUM
Generic NameNatrum Salicylicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSODIUM SALICYLATE
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0311-0

100 PELLET in 1 PACKAGE (15631-0311-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0311-1 [15631031101]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0311-3 [15631031103]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0311-2 [15631031102]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0311-0 [15631031100]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0311-4 [15631031104]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0311-5 [15631031105]

NATRUM SALICYLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
SODIUM SALICYLATE2 [hp_X]/1

OpenFDA Data

SPL SET ID:f0959b77-989b-4309-9c3a-4e099b4c7d1b
Manufacturer
UNII

NDC Crossover Matching brand name "NATRUM SALICYLICUM" or generic name "Natrum Salicylicum"

NDCBrand NameGeneric Name
15631-0311NATRUM SALICYLICUMNATRUM SALICYLICUM
37662-1147Natrum SalicylicumNatrum Salicylicum
37662-1148Natrum SalicylicumNatrum Salicylicum
37662-1149Natrum SalicylicumNatrum Salicylicum
37662-1150Natrum SalicylicumNatrum Salicylicum
37662-1151Natrum SalicylicumNatrum Salicylicum
37662-1152Natrum SalicylicumNatrum Salicylicum
37662-1153Natrum SalicylicumNatrum Salicylicum
68428-528Natrum salicylicumSODIUM SALICYLATE
71919-486Natrum salicylicumSODIUM SALICYLATE

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