LAMIUM ALBUM 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 Lamium Album.
Product ID | 15631-0265_60846b38-f413-4dbe-a161-7878f9d138a7 |
NDC | 15631-0265 |
Product Type | Human Otc Drug |
Proprietary Name | LAMIUM ALBUM |
Generic Name | Lamium Album |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2015-09-05 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
Substance Name | LAMIUM ALBUM |
Active Ingredient Strength | 1 [hp_X]/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2018-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2018-01-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-03-23 |
Ingredient | Strength |
---|---|
LAMIUM ALBUM | 1 [hp_X]/1 |
SPL SET ID: | 05a57d4f-2fe2-43ec-a561-7e75fd450b91 |
Manufacturer | |
UNII |