Ambra grisea is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Ambergris.
Product ID | 68428-195_7e3e06c4-b001-5d77-e053-2991aa0a7cec |
NDC | 68428-195 |
Product Type | Human Otc Drug |
Proprietary Name | Ambra grisea |
Generic Name | Ambergris |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2010-04-29 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | AMBERGRIS |
Active Ingredient Strength | 30 [hp_C]/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2010-04-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-04-29 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-04-29 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-04-29 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-04-29 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-04-29 |
Ingredient | Strength |
---|---|
AMBERGRIS | 30 [hp_C]/1 |
SPL SET ID: | 851ac4b6-ccea-474a-bc7e-33c3e5497799 |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0220-0221 | Ambra grisea | AMBERGRIS |
15631-0023 | AMBRA GRISEA | AMBRA GRISEA |
60512-7101 | AMBRA GRISEA | AMBRA GRISEA |
68428-195 | Ambra grisea | AMBERGRIS |
71919-037 | Ambra grisea | AMBERGRIS |
64117-105 | Nervous Cough | AMBERGRIS |