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Many of Over the Counter drugs are not reviewed by the FDA but they might be marketed to the public if the product complies with the applicable rules and regulations. This site is not affiliated, endorsed or administered by the Food and Drug Administration (FDA). Reliance on any information provided by the National Drug Codes List website or other visitors to this website is solely at your own risk. The contents of the National Drug Codes List website are provided for educational purposes only and are not intended in any way as medical advice, medical diagnosis or treatment. NDC List 2022 | NDC Data Last Updated: 06-01-2022Īll contents of this website are provided on an "as is" and "as available" basis without warranty of any kind. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I").
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This is the date when the listing record will expire if not updated or certified by the product labeler.Įxclude Flag: N - NO What is the NDC Exclude Flag? Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date? This is the date that the labeler indicates was the start of its marketing of the drug product. Start Marketing Date: 06-28-2018 What is the Start Marketing Date? The complete list of codes and translations can be found at under Structured Product Labeling Resources. Currently, only final marketed product categories are included. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. For unapproved drugs, this field will be null. 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. This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated.
#AER WITCH HAZEL PADS CODE#
Name of Company corresponding to the labeler code segment of the Product NDC.įDA Application Number: part346 What is the FDA Application Number? Product Labeler Information What is the Labeler Name? 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 translation of the route code submitted by the firm, indicating route of administration. ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)Īdministration Route(s) What are the Administration Route(s)?.BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7).The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). Inactive Ingredient(s) About the Inactive Ingredient(s) Each ingredient name is the preferred term of the UNII code submitted. This data element matches the “Document Type” field of the Structured Product Listing.Īer Pre-moistened Witch Hazel Pad Active Ingredient(s) What is the Active Ingredient(s) List? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. Product Type: Human Otc Drug What kind of product is this? The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1247779.ĭosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents. The product's dosage form is solution and is administered via rectal topical form. The generic name of Aer Pre-moistened Witch Hazel Pad is witch hazel. Aer Pre-moistened Witch Hazel Pad with NDC 50289-3250 is a a human over the counter drug product labeled by Birchwood Laboratories Llc.