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NDC 69683-0101-11 DERMOSCRIBE ICHYBUM 1; 1 g/100g; g/100g Details
DERMOSCRIBE ICHYBUM 1; 1 g/100g; g/100g
DERMOSCRIBE ICHYBUM is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by DERMOSCRIBE PTY LTD. The primary component is CLIOQUINOL; HYDROCORTISONE.
MedlinePlus Drug Summary
Clioquinol is used to treat skin infections such as eczema, athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 69683-0101-11Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Clioquinol Topical
Hydrocortisone topical is used to treat redness, swelling, itching, and discomfort of various skin conditions. 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: 69683-0101-11Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydrocortisone Topical
Product Information
| NDC | 69683-0101 |
|---|---|
| Product ID | 69683-101_06d42f39-2499-7b3d-e063-6294a90ab05c |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | DERMOSCRIBE ICHYBUM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | HYDROCORTISONE, CLIOQUINOL, ZINC OXIDE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 1; 1 |
| Active Ingredient Units | g/100g; g/100g |
| Substance Name | CLIOQUINOL; HYDROCORTISONE |
| Labeler Name | DERMOSCRIBE PTY LTD |
| Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part348 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69683-0101-11 (69683010111)
| NDC Package Code | 69683-101-11 |
|---|---|
| Billing NDC | 69683010111 |
| Package | 28 g in 1 BOTTLE (69683-101-11) |
| Marketing Start Date | 2015-03-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |