NDC 15631-0305

NAPHTHALINUM

Naphthalinum

NAPHTHALINUM 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 Naphthalene.

Product ID15631-0305_81df9d9b-e982-4db8-a4bb-339b813651db
NDC15631-0305
Product TypeHuman Otc Drug
Proprietary NameNAPHTHALINUM
Generic NameNaphthalinum
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 NameNAPHTHALENE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0305-0

100 PELLET in 1 PACKAGE (15631-0305-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0305-5 [15631030505]

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

NDC 15631-0305-3 [15631030503]

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

NDC 15631-0305-1 [15631030501]

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

NDC 15631-0305-2 [15631030502]

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

NDC 15631-0305-0 [15631030500]

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

NDC 15631-0305-4 [15631030504]

NAPHTHALINUM 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
NAPHTHALENE3 [hp_X]/1

OpenFDA Data

SPL SET ID:56d1b7a4-481c-4381-a473-b43ada697936
Manufacturer
UNII

NDC Crossover Matching brand name "NAPHTHALINUM" or generic name "Naphthalinum"

NDCBrand NameGeneric Name
0220-3553NaphthalinumNAPHTHALENE
15631-0305NAPHTHALINUMNAPHTHALINUM
68428-521NaphthalinumNAPHTHALENE
71919-477NaphthalinumNAPHTHALENE

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