NDC 69646-705
ALCORTIN A
Iodoquinol, Hydrocortisone Acetate And Aloe Vera Leaf
ALCORTIN A is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Novum Pharma, Llc. The primary component is Iodoquinol; Hydrocortisone Acetate; Aloe Vera Leaf.
| Product ID | 69646-705_13338200-260d-48f0-aeae-50fff077a3b9 |
| NDC | 69646-705 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ALCORTIN A |
| Generic Name | Iodoquinol, Hydrocortisone Acetate And Aloe Vera Leaf |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2015-03-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Novum Pharma, LLC |
| Substance Name | IODOQUINOL; HYDROCORTISONE ACETATE; ALOE VERA LEAF |
| Active Ingredient Strength | 10 mg/g; mg/g; mg/g |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
Packaging
NDC 69646-705-02
2 g in 1 PACKET (69646-705-02)
| Marketing Start Date | 2015-03-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 69646-705-08 [69646070508]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-03-01 |
NDC 69646-705-11 [69646070511]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-16 |
NDC 69646-705-02 [69646070502]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-03-01 |
NDC 69646-705-03 [69646070503]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-16 |
NDC 69646-705-15 [69646070515]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2015-03-01 |
NDC 69646-705-13 [69646070513]
ALCORTIN A GEL
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2015-03-01 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| IODOQUINOL | 10 mg/g |
OpenFDA Data
| SPL SET ID: | 0a1a6d71-2295-4f83-a597-c477cafc56f7 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Pharmacological Class
- Corticosteroid [EPC]
- Corticosteroid Hormone Receptor Agonists [MoA]
NDC Crossover Matching brand name "ALCORTIN A" or generic name "Iodoquinol, Hydrocortisone Acetate And Aloe Vera Leaf"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 68040-705 | Alcortin A | HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol |
| 69646-705 | ALCORTIN A | iodoquinol, hydrocortisone acetate and aloe vera leaf |
Trademark Results [ALCORTIN A]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ALCORTIN A 85226797 4015701 Live/Registered |
NOVUM PHARMA, LLC 2011-01-26 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.