Search by Drug Name or NDC
NDC 70403-0923-30 HYDROCORTISONE MAXIMUM STRENGTH 10 mg/g Details
HYDROCORTISONE MAXIMUM STRENGTH 10 mg/g
HYDROCORTISONE MAXIMUM STRENGTH is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Aru Pharma Inc.. The primary component is HYDROCORTISONE.
MedlinePlus Drug Summary
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: 70403-0923-30Last Updated: 05/05/2024
MedLinePlus Full Drug Details: Hydrocortisone Topical
Product Information
NDC | 70403-0923 |
---|---|
Product ID | 70403-923_435da8cc-a197-4520-a760-06e0c310628b |
Associated GPIs | 90550075003720 |
GCN Sequence Number | 007544 |
GCN Sequence Number Description | hydrocortisone CREAM (G) 1 % TOPICAL |
HIC3 | Q5P |
HIC3 Description | TOPICAL ANTI-INFLAMMATORY STEROIDAL |
GCN | 30942 |
HICL Sequence Number | 002867 |
HICL Sequence Number Description | HYDROCORTISONE |
Brand/Generic | Generic |
Proprietary Name | HYDROCORTISONE MAXIMUM STRENGTH |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Hydrocortisone |
Product Type | HUMAN OTC DRUG |
Dosage Form | CREAM |
Route | TOPICAL |
Active Ingredient Strength | 10 |
Active Ingredient Units | mg/g |
Substance Name | HYDROCORTISONE |
Labeler Name | Aru Pharma Inc. |
Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH NOT FINAL |
Application Number | part348 |
Listing Certified Through | n/a |
Package
NDC 70403-0923-30 (70403092330)
NDC Package Code | 70403-923-30 |
---|---|
Billing NDC | 70403092330 |
Package | 1 TUBE in 1 CARTON (70403-923-30) / 30 g in 1 TUBE |
Marketing Start Date | 2018-01-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |