NDC 15631-0231

ICHTHYOLUM

Ichthyolum

ICHTHYOLUM 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 Ichthammol.

Product ID15631-0231_0f1a6e9e-7b9f-4805-b300-1541037342f2
NDC15631-0231
Product TypeHuman Otc Drug
Proprietary NameICHTHYOLUM
Generic NameIchthyolum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameICHTHAMMOL
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0231-0

100 PELLET in 1 PACKAGE (15631-0231-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0231-0 [15631023100]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0231-2 [15631023102]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0231-4 [15631023104]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0231-1 [15631023101]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0231-5 [15631023105]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0231-3 [15631023103]

ICHTHYOLUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
ICHTHAMMOL3 [hp_X]/1

OpenFDA Data

SPL SET ID:4d5d0256-ffba-4cd8-bdad-29afd66c3e37
Manufacturer
UNII

NDC Crossover Matching brand name "ICHTHYOLUM" or generic name "Ichthyolum"

NDCBrand NameGeneric Name
15631-0231ICHTHYOLUMICHTHYOLUM
68428-956IchthyolumICHTHAMMOL
71919-356IchthyolumICHTHAMMOL

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