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NDC 11086-0032-01 VANOXIDE 5; .5 g/100g; g/100g Details
VANOXIDE 5; .5 g/100g; g/100g
VANOXIDE is a TOPICAL LOTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Summers Laboratories Inc. The primary component is BENZOYL PEROXIDE; HYDROCORTISONE.
MedlinePlus Drug Summary
Benzoyl peroxide is used to treat mild to moderate acne.
Related Packages: 11086-0032-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Benzoyl Peroxide 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: 11086-0032-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Hydrocortisone Topical
Product Information
| NDC | 11086-0032 |
|---|---|
| Product ID | 11086-032_074cfc73-ce31-5fe4-e063-6394a90a307a |
| Associated GPIs | 90059902144110 |
| GCN Sequence Number | 064802 |
| GCN Sequence Number Description | benzoyl peroxide/hydrocortison SUSPENSION 5 %-0.5 % TOPICAL |
| HIC3 | L5O |
| HIC3 Description | KERATOLYTIC-GLUCOCORTICOID COMBINATIONS |
| GCN | 16498 |
| HICL Sequence Number | 003292 |
| HICL Sequence Number Description | BENZOYL PEROXIDE/HYDROCORTISONE |
| Brand/Generic | Brand |
| Proprietary Name | VANOXIDE |
| Proprietary Name Suffix | HC |
| Non-Proprietary Name | BENZOYL PEROXIDE, HYDROCORTISONE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | LOTION |
| Route | TOPICAL |
| Active Ingredient Strength | 5; .5 |
| Active Ingredient Units | g/100g; g/100g |
| Substance Name | BENZOYL PEROXIDE; HYDROCORTISONE |
| Labeler Name | Summers Laboratories Inc |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 11086-0032-01 (11086003201)
| NDC Package Code | 11086-032-01 |
|---|---|
| Billing NDC | 11086003201 |
| Package | 25 g in 1 BOTTLE (11086-032-01) |
| Marketing Start Date | 2009-11-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |