NDC 0220-2395

Hekla lava

Hekla Lava

Hekla lava is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Hekla Lava.

Product ID0220-2395_85b57210-6007-01ba-e053-2991aa0a1197
NDC0220-2395
Product TypeHuman Otc Drug
Proprietary NameHekla lava
Generic NameHekla Lava
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameHEKLA LAVA
Active Ingredient Strength200 [kp_C]/200[kp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-2395-41

200 [kp_C] in 1 TUBE (0220-2395-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-2395-41 [00220239541]

Hekla lava PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
HEKLA LAVA200 [kp_C]/200[kp_C]

OpenFDA Data

SPL SET ID:85b57210-6006-01ba-e053-2991aa0a1197
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

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