NDC 66096-728 Dandruff Relief

Baptisia Tinctoria, Borax, Calendula, Candida Albicans, Eugenia Caryophyllata, Fucus Vesiculosus, Kali Iodatum, Symphytum Officinale, Thuja Occidentalis.

NDC Product Code 66096-728

NDC CODE: 66096-728

Proprietary Name: Dandruff Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Baptisia Tinctoria, Borax, Calendula, Candida Albicans, Eugenia Caryophyllata, Fucus Vesiculosus, Kali Iodatum, Symphytum Officinale, Thuja Occidentalis. What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Potassium iodide is used to loosen and break up mucus in the airways. This helps you cough up the mucus so you can breathe more easily if you have long-term lung problems (e.g., asthma, chronic bronchitis, emphysema). This medication is known as an expectorant. Potassium iodide is also used along with antithyroid medicines to prepare the thyroid gland for surgical removal, to treat certain overactive thyroid conditions (hyperthyroidism), and to protect the thyroid in a radiation exposure emergency. It works by shrinking the size of the thyroid gland and decreasing the amount of thyroid hormones produced. In a radiation emergency, potassium iodide blocks only the thyroid from absorbing radioactive iodine, protecting it from damage and reducing the risk of thyroid cancer. Use this medication along with other emergency measures that will be recommended to you by public health and safety officials (e.g., finding safe shelter, evacuation, controlling food supply).

NDC Code Structure

  • 66096 - Ohm Pharma Inc.

NDC 66096-728-08

Package Description: 240 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Dandruff Relief with NDC 66096-728 is a a human over the counter drug product labeled by Ohm Pharma Inc.. The generic name of Dandruff Relief is baptisia tinctoria, borax, calendula, candida albicans, eugenia caryophyllata, fucus vesiculosus, kali iodatum, symphytum officinale, thuja occidentalis.. The product's dosage form is shampoo and is administered via topical form.

Labeler Name: Ohm Pharma Inc.

Dosage Form: Shampoo - A liquid soap or detergent used to clean the hair and scalp and is often used as a vehicle for dermatologic agents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Dandruff Relief Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BAPTISIA TINCTORIA ROOT 1 [hp_X]/240mL
  • SODIUM BORATE 1 [hp_X]/240mL
  • CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/240mL
  • CANDIDA ALBICANS 30 [hp_X]/240mL
  • CLOVE 1 [hp_X]/240mL
  • FUCUS VESICULOSUS 1 [hp_X]/240mL
  • POTASSIUM IODIDE 2 [hp_X]/240mL
  • COMFREY ROOT 6 [hp_X]/240mL
  • THUJA OCCIDENTALIS LEAFY TWIG 1 [hp_X]/240mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • COCAMIDE (UNII: 3YXD33R71G)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
  • DISODIUM LAURYL SULFOSUCCINATE (UNII: P160Q81342)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • OREGANO LEAF OIL (UNII: 7D0CGR40U1)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • WATER (UNII: 059QF0KO0R)
  • SESAME OIL (UNII: QX10HYY4QV)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • WHEAT GERM OIL (UNII: 14C97E680P)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ohm Pharma Inc.
Labeler Code: 66096
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 11-02-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Dandruff Relief Product Label Images