NDC 15631-0218

HEKLA LAVA

Hekla Lava

HEKLA LAVA 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 Hekla Lava.

Product ID15631-0218_0edf30a1-99f0-446a-90bd-b594b0e93b01
NDC15631-0218
Product TypeHuman Otc Drug
Proprietary NameHEKLA LAVA
Generic NameHekla Lava
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameHEKLA LAVA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0218-0

100 PELLET in 1 PACKAGE (15631-0218-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0218-1 [15631021801]

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

NDC 15631-0218-4 [15631021804]

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

NDC 15631-0218-0 [15631021800]

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

NDC 15631-0218-3 [15631021803]

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

NDC 15631-0218-2 [15631021802]

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

NDC 15631-0218-5 [15631021805]

HEKLA LAVA 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
HEKLA LAVA1 [hp_X]/1

OpenFDA Data

SPL SET ID:0ffb0c23-fa2e-4fb0-992c-0451d545acb7
Manufacturer
UNII

NDC Crossover Matching brand name "HEKLA LAVA" or generic name "Hekla Lava"

NDCBrand NameGeneric Name
0220-2391Hekla lavaHEKLA LAVA
0220-2392Hekla lavaHEKLA LAVA
0220-2393Hekla lavaHEKLA LAVA
0220-2394Hekla lavaHEKLA LAVA
0220-2395Hekla lavaHEKLA LAVA
0220-2396Hekla lavaHEKLA LAVA
0220-2397Hekla lavaHEKLA LAVA
0220-2428Hekla lavaHEKLA LAVA
15631-0218HEKLA LAVAHEKLA LAVA
62106-5062HEKLA LAVAHekla lava
68428-421Hekla lavaHEKLA LAVA
71919-335Hekla lavaHEKLA LAVA
64117-147Toothache NeuralgiaHEKLA LAVA

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