NDC 15631-0103

CAMPHORA

Camphora

CAMPHORA 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 Camphor (natural).

Product ID15631-0103_1809ed3a-b684-4c7e-9621-b1867660fb79
NDC15631-0103
Product TypeHuman Otc Drug
Proprietary NameCAMPHORA
Generic NameCamphora
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCAMPHOR (NATURAL)
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0103-0

100 PELLET in 1 PACKAGE (15631-0103-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0103-0 [15631010300]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0103-2 [15631010302]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0103-3 [15631010303]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0103-4 [15631010304]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0103-5 [15631010305]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0103-1 [15631010301]

CAMPHORA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
CAMPHOR (NATURAL)1 [hp_X]/1

OpenFDA Data

SPL SET ID:09826ded-6084-4274-b694-6ce21cca9586
Manufacturer
UNII

NDC Crossover Matching brand name "CAMPHORA" or generic name "Camphora"

NDCBrand NameGeneric Name
0220-1121CamphoraCAMPHOR (NATURAL)
0220-1122CamphoraCAMPHOR (NATURAL)
0220-5349CamphoraCAMPHOR (NATURAL)
15631-0103CAMPHORACAMPHORA
53645-1800CamphoraCamphora
53645-1801CamphoraCamphora
53645-1930CamphoraCamphora
66096-808CamphoraCAMPHORA
68428-282CamphoraCAMPHOR (NATURAL)
71919-155CamphoraCAMPHOR (NATURAL)
69152-1108Camphora 200CCamphora

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.