NDC 0220-2428

Hekla lava

Hekla Lava

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

• Product ID: 0220-2428_5f9ed8a7-90eb-0fd6-e053-2991aa0ad919
• NDC: 0220-2428
• Product Type: Human Otc Drug
• Proprietary Name: Hekla lava
• Generic Name: Hekla Lava
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Laboratoires Boiron
• Substance Name: HEKLA LAVA
• Active Ingredient Strength: 8 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-2428-41

80 PELLET in 1 TUBE (0220-2428-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-2428-41 [00220242841]

Hekla lava PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
HEKLA LAVA	8 [hp_X]/1

OpenFDA Data

• SPL SET ID: c31c8340-7c5c-11e6-8542-424c58303031
• Manufacturer:
  • Laboratoires Boiron
• UNII:
  • C21158IIRK

NDC Crossover Matching brand name "Hekla lava" or generic name "Hekla Lava"

NDC	Brand Name	Generic Name
0220-2391	Hekla lava	HEKLA LAVA
0220-2392	Hekla lava	HEKLA LAVA
0220-2393	Hekla lava	HEKLA LAVA
0220-2394	Hekla lava	HEKLA LAVA
0220-2395	Hekla lava	HEKLA LAVA
0220-2396	Hekla lava	HEKLA LAVA
0220-2397	Hekla lava	HEKLA LAVA
0220-2428	Hekla lava	HEKLA LAVA
15631-0218	HEKLA LAVA	HEKLA LAVA
62106-5062	HEKLA LAVA	Hekla lava
68428-421	Hekla lava	HEKLA LAVA
71919-335	Hekla lava	HEKLA LAVA
64117-147	Toothache Neuralgia	HEKLA LAVA