Herb Street Anti-itch Stick
Hydrocortisone
Balassa Laboratories Inc.
Human Otc Drug
NDC 10107-429Herb Street Anti-itch Stick also known as Hydrocortisone is a human otc drug labeled by 'Balassa Laboratories Inc.'. National Drug Code (NDC) number for Herb Street Anti-itch Stick is 10107-429. This drug is available in dosage form of Stick. The names of the active, medicinal ingredients in Herb Street Anti-itch Stick drug includes Hydrocortisone - .01 g/g . The currest status of Herb Street Anti-itch Stick drug is Active.
Drug Information:
| Drug NDC: | 10107-429 |
| 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: | Herb Street Anti-itch Stick |
| 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 |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Balassa Laboratories Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Stick |
| 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 - .01 g/g
|
| 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: | 01 May, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 12 Jun, 2026 |
| 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: | 31 Dec, 2023 |
| 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: | Balassa Laboratories Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| 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 |
|---|
| 10107-429-02 | 1 TUBE in 1 CARTON (10107-429-02) / 16.8 g in 1 TUBE (10107-429-01) | 01 May, 2022 | N/A | 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 anti-itch
Product Elements:
Herb street anti-itch stick hydrocortisone hydrocortisone hydrocortisone yellow wax avocado oil soybean oil castor oil cannabis sativa seed oil glycerin phenoxyethanol .alpha.-tocopherol acetate aloe vera leaf ethylhexylglycerin
Indications and Usage:
Uses for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to: eczema insect bites poison ivy, poison oak, or poison sumac seborrheic dermatitis psoriasis other uses of this product should only be under the advice and supervision of a doctor.
Warnings:
Warnings for external use only do not use for the treatment of diaper rash. consult a doctor. when using this product use only as directed avoid contact with eyes stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days if you need to stop use of the product because of the above, do not begin use of any other hydrocortisone product unless you have consulted a doctor. if pregnant or breast-feeding ask a healthcare professional before use. keep out of reach of children. if swallowed, get medical help or contact a poison control center immediately.
Do Not Use:
Warnings for external use only do not use for the treatment of diaper rash. consult a doctor. when using this product use only as directed avoid contact with eyes stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days if you need to stop use of the product because of the above, do not begin use of any other hydrocortisone product unless you have consulted a doctor. if pregnant or breast-feeding ask a healthcare professional before use. keep out of reach of children. if swallowed, get medical help or contact a poison control center immediately.
When Using:
When using this product use only as directed avoid contact with eyes
Dosage and Administration:
Directions adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. children under 2 years of age: do not use; consult a doctor.
Stop Use:
Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days if you need to stop use of the product because of the above, do not begin use of any other hydrocortisone product unless you have consulted a doctor.
Package Label Principal Display Panel:
Principal display panel - 16.8 g tube in carton herb street with hemp seed oil moisturizer anti-itch stick 1% hydrocortisone topical analgesic stick net wt 0.59 oz (16.8 g) no mess stick money back guranteed manufactured by balassa laboratories, inc. po box 291161, port orange, fl 32129 made in the usa from us and imported materials all rights reserved. all copyrights and trademarks are owned by balassa laboratories, inc. 10107-431-02 carton