Home Health Everclean Antidandruff
Salicylic Acid
Home Health
Human Otc Drug
NDC 76020-200Home Health Everclean Antidandruff also known as Salicylic Acid is a human otc drug labeled by 'Home Health'. National Drug Code (NDC) number for Home Health Everclean Antidandruff is 76020-200. This drug is available in dosage form of Shampoo. The names of the active, medicinal ingredients in Home Health Everclean Antidandruff drug includes Salicylic Acid - 1.8 g/100mL . The currest status of Home Health Everclean Antidandruff drug is Active.
Drug Information:
| Drug NDC: | 76020-200 |
| 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: | Home Health Everclean Antidandruff |
| 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: | Salicylic Acid |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Home Health |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Shampoo |
| 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: | SALICYLIC ACID - 1.8 g/100mL
|
| 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 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: | 14 Feb, 2011 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 23 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: | part358H |
| 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: | Home Health
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 205173
1091403
|
| 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: | 0318858546244
|
| UPC stands for Universal Product Code. |
| UNII: | O414PZ4LPZ
|
| 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. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 76020-200-08 | 1 BOTTLE in 1 CARTON (76020-200-08) / 236 mL in 1 BOTTLE | 08 Feb, 2017 | 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:
Uses for relief oil; itching and scalp falking associated with dandruff, seborrheic dermatitis and psoriasis
Product Elements:
Home health everclean antidandruff salicylic acid allantoin aloe vera leaf cholecalciferol corn oil glycerin pummelo lawsonia inermis leaf honey hops lauric diethanolamide chamomile urtica dioica leaf panthenol propylene glycol vitamin a palmitate rosemary sodium chloride triethanolamine lauryl sulfate tea tree oil trolamine water salicylic acid salicylic acid
Indications and Usage:
When using this product avoid contact with eyes. if contact occurs, rinse eyes thoroughly with water.
Warnings:
Warnings for external use only.
Dosage and Administration:
Directions -shake well before use -wet hair thoroughly -lather, rinse and repeat -for best results use at least twice a week or as directed by a doctor
Stop Use:
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.
Description:
Prod. no. 54624 everclean shampoo helps eliminate itching and scalp flacking associated with dandruff, psoriasis and seborrheic dermatitis, the active ingredient salicylic acid combines with a nutrient-filled moisturizing base that includes; -tea tree oil - traditional ingredient used for natural cleansing -aloe vera - a moisturizer for the scalp and hair - allantoin - to soothe and improve scalp condition - vegetable protein - to add body and sheen to the hair - natural pine tar - a cleansing agent that leaves a fresh pine scent - panthenol - to nourish and strengthen the hair while increasing luster - vitamins a and d - essential nutrients for scalp and hair - plus gentle herbal extracts of chamomile, henna, hops, horsetail, nettle and rosemary free of preservatives, parabens, mineral oil, petroleum, animal materials and artificial colors. 3 18858 54624 4 carefully manufactured for home health,co. ronkonkoma, ny 11779 u.s.a. www.homehealthus.com b54624 c2010 home health 02b
Package Label Principal Display Panel:
Homehealth natural health begins at home everclean antidandruff shampoo salicyclic acid with tea tree oil, aloe vera, allantoin and herbal extracts - for relief of itching and scalp flaking associated with dandruff, psoriasis and seborrheic dermatitis. - gentle, moisturizing shampoo -leaves hair fresh, healthy and manageable - contains no artificial preservatives or colors - paraben-free net wt. 8 fl. oz (236 ml)
Everclean antidandruff shampoo