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NDC 59088-0430-05 Lidocort 5; 30 mg/g; mg/g Details
Lidocort 5; 30 mg/g; mg/g
Lidocort is a RECTAL; TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PureTek Corporation. The primary component is HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Rectal hydrocortisone is used along with other medications to treat proctitis (swelling in the rectum) and ulcerative colitis (a condition which causes swelling and sores in the lining of the large intestine and rectum). It is also used to relieve itching and swelling from hemorrhoids and other rectal problems. Hydrocortisone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
Related Packages: 59088-0430-05Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydrocortisone Rectal
Product Information
| NDC | 59088-0430 |
|---|---|
| Product ID | 59088-430_f204edc7-fadd-5b36-e053-2a95a90af89b |
| Associated GPIs | 89991002263720 |
| GCN Sequence Number | 047968 |
| GCN Sequence Number Description | lidocaine/hydrocortisone ac CREAM (G) 3 %-0.5 % TOPICAL |
| HIC3 | T0F |
| HIC3 Description | TOPICAL ANTI-INFLAMMATORY STEROID-LOCAL ANESTHETIC |
| GCN | 13397 |
| HICL Sequence Number | 022142 |
| HICL Sequence Number Description | LIDOCAINE HCL/HYDROCORTISONE ACETATE |
| Brand/Generic | Generic |
| Proprietary Name | Lidocort |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | LIDOCAINE HCL - HYDROCORTISONE ACETATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CREAM |
| Route | RECTAL; TOPICAL |
| Active Ingredient Strength | 5; 30 |
| Active Ingredient Units | mg/g; mg/g |
| Substance Name | HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE |
| Labeler Name | PureTek Corporation |
| Pharmaceutical Class | Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Local Anesthesia [PE] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59088-0430-05 (59088043005)
| NDC Package Code | 59088-430-05 |
|---|---|
| Billing NDC | 59088043005 |
| Package | 85 g in 1 TUBE (59088-430-05) |
| Marketing Start Date | 2020-09-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |