lidocaine hydrochloride and hydrocortisone acetate

Generic: lidocaine hydrochloride and hydrocortisone acetate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride and hydrocortisone acetate
Generic Name lidocaine hydrochloride and hydrocortisone acetate
Labeler westminster pharmaceuticals, llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

hydrocortisone acetate 5 mg/g, lidocaine hydrochloride 30 mg/g

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-397
Product ID 69367-397_7cb595ac-4371-425c-9da9-c26a9d9ec9a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2027-12-31
Marketing Start 2024-11-15

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] corticosteroid hormone receptor agonists [moa] corticosteroid [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367397
Hyphenated Format 69367-397

Supplemental Identifiers

RxCUI
1012235
UNII
3X7931PO74 V13007Z41A

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lidocaine hydrochloride and hydrocortisone acetate (source: ndc)
Generic Name lidocaine hydrochloride and hydrocortisone acetate (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/g
  • 30 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (69367-397-01) / 28.35 g in 1 TUBE
  • 1 TUBE in 1 CARTON (69367-397-85) / 85 g in 1 TUBE
source: ndc

Packages (2)

Ingredients (2)

hydrocortisone acetate (5 mg/g) lidocaine hydrochloride (30 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "7cb595ac-4371-425c-9da9-c26a9d9ec9a3", "openfda": {"unii": ["3X7931PO74", "V13007Z41A"], "rxcui": ["1012235"], "spl_set_id": ["0cd1394d-e7b2-4e60-87ac-e12a0bda9d67"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69367-397-01)  / 28.35 g in 1 TUBE", "package_ndc": "69367-397-01", "marketing_start_date": "20241115"}, {"sample": false, "description": "1 TUBE in 1 CARTON (69367-397-85)  / 85 g in 1 TUBE", "package_ndc": "69367-397-85", "marketing_start_date": "20241115"}], "brand_name": "Lidocaine Hydrochloride and Hydrocortisone Acetate", "product_id": "69367-397_7cb595ac-4371-425c-9da9-c26a9d9ec9a3", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "Local Anesthesia [PE]"], "product_ndc": "69367-397", "generic_name": "Lidocaine Hydrochloride and Hydrocortisone Acetate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride and Hydrocortisone Acetate", "active_ingredients": [{"name": "HYDROCORTISONE ACETATE", "strength": "5 mg/g"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "30 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20241115", "listing_expiration_date": "20271231"}