Opuntia vulgaris is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Opuntia Ficus-indica.
Product ID | 68428-544_75e0ab17-3208-517f-e053-2a91aa0affc1 |
NDC | 68428-544 |
Product Type | Human Otc Drug |
Proprietary Name | Opuntia vulgaris |
Generic Name | Opuntia Ficus-indica |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2010-08-03 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Washington Homeopathic Products |
Substance Name | OPUNTIA FICUS-INDICA |
Active Ingredient Strength | 30 [hp_C]/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2010-08-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-03 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-08-03 |
Ingredient | Strength |
---|---|
OPUNTIA FICUS-INDICA | 30 [hp_C]/1 |
SPL SET ID: | 4c07385b-d0d0-402a-91de-0259a1bb1e4d |
Manufacturer | |
UNII | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
15631-0322 | OPUNTIA VULGARIS | OPUNTIA VULGARIS |
68428-544 | Opuntia vulgaris | OPUNTIA FICUS-INDICA |
71919-507 | Opuntia vulgaris | OPUNTIA FICUS-INDICA |