Hydrocortisone
Hydrocortisone Cream
Mckesson
Human Otc Drug
NDC 68599-1182Hydrocortisone also known as Hydrocortisone Cream is a human otc drug labeled by 'Mckesson'. National Drug Code (NDC) number for Hydrocortisone is 68599-1182. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Hydrocortisone drug includes Hydrocortisone - 1 g/100g . The currest status of Hydrocortisone drug is Active.
Drug Information:
| Drug NDC: | 68599-1182 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Hydrocortisone |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Hydrocortisone Cream |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Mckesson |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cream |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | HYDROCORTISONE - 1 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 13 Mar, 2019 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 01 Jul, 2024 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part348 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 24 Dec, 2025 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | McKesson
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 106258
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0612479243507
|
| UPC stands for Universal Product Code. |
| NUI: | N0000175576
N0000175450
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | WI4X0X7BPJ
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
| Pharmacologic Class MOA: | Corticosteroid Hormone Receptor Agonists [MoA]
|
| Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`. |
| Pharmacologic Class EPC: | Corticosteroid [EPC]
|
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. |
| Pharmacologic Class: | Corticosteroid Hormone Receptor Agonists [MoA]
Corticosteroid [EPC]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 68599-1182-2 | .9 g in 1 PACKET (68599-1182-2) | 14 Mar, 2019 | 01 Jul, 2024 | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose antipruritic (anti itch)
Product Elements:
Hydrocortisone hydrocortisone cream citric acid monohydrate polysorbate 80 trisodium citrate dihydrate glycerin glyceryl monostearate methylparaben mineral oil phenoxyethanol benzoic acid water titanium dioxide chlorphenesin petrolatum hydrocortisone hydrocortisone
Indications and Usage:
Indications: for the temporary relief of itching associated with minor skin irritation and rashes due to eczema, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, jewelry, seborrheic dermatitis, psoriasis scrapes for the temporary relief of external genital, feminine and anal itching other uses of this product should be only under the advice and supervision of a doctor
Warnings:
Warnings: for external use only avoid contact with eyes do not exceed the recommended daily dosage unless directed by a doctor do no use for treatment of diaper rash in case of bleeding, consult a doctor promptly consult a doctor: before use if you have a vaginal discharge (for external feminine itching) for external itching, do not exceed the recommended daily dosage or if bleeding occurs if condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days discontinue use of this product when using this product: do not put this product into rectum by using fingers or any mechanical device or applicator
Dosage and Administration:
Directions: for adults and children 2 years of age and older: apply externally to affected area not more than 3 to 4 times daily. children under 2 years of age: do not use, consult a doctor adults for external anal itching when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly, or by patting or blotting with appropriate cleansing pad. gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. children under 12 years or age; for external anal itching, consult a doctor.
Stop Use:
Do not use: with any other hydrocortisone product unless you have consulted a doctor
Package Label Principal Display Panel:
Ndc 68599-1182-2 hydrocortisone cream 1% maximum strength effective itch and rash relief cream. net weight 0.9 g (0.03 oz) mfr # 118-82464 118-82464 each
Ndc 68599-1182-2 mckesson hydrocortisone cream 1% maximum strength net weight 0.9 g (0.03 oz) 144 packs per box mfr # 118-82464 118-82464 box
Ndc 68599-1182-2 mckesson hydrocortisone cream 1% maximum strength net weight 0.9 g (0.03 oz) 144 packs per box 12 boxes per case mfr # 118-82464 118-82464 case
Further Questions:
Questions? call 1-800-777-4908