- #L227 RED PILL SKIN#
- #L227 RED PILL CODE#
Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-80). These could be signs of a serious condition. fever gets worse or lasts more than 3 days.pain gets worse or lasts more than 10 days.if you have ever had an allergic reaction to this product or any of its ingredientsĪsk A Doctor Or Pharmacist Before Use If You Are.If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. with any other drug containing acetaminophen (prescription or nonprescription).
#L227 RED PILL SKIN#
If a skin reaction occurs, stop use and seek medical help right away.
3 or more alcoholic drinks every day while using this productĪllergy alert: Acetaminophen may cause severe skin reactions. with other drugs containing acetaminophen. more than 4,000 mg of acetaminophen in 24 hours. Severe liver damage may occur if you take Liver warning: This product contains acetaminophen. temporarily relieves minor aches and pains due to:. ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc. Values = "Y", "N", "E", or "I".įDA filings in the form of structured product labels are documents that include all published material associated whith this product. 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"). This is the date when the listing record will expire if not updated or certified by the product labeler.Įxclude Flag What is the NDC Exclude Flag? Listing Expiration Date 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 What is the Start Marketing Date? OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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 What is the Marketing Category? 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. #L227 RED PILL CODE#
Name of Company corresponding to the labeler code segment of the Product NDC.įDA Application Number What is the FDA Application Number? Product Labeler Information What is the Labeler Name? Oral - Administration to or by way of the mouth.The translation of the route code submitted by the firm, indicating route of administration. Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.Īdministration Route(s) What are the Administration Route(s)? This data element matches the “Document Type” field of the Structured Product Listing. Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug.
Product Type What kind of product is this? The generic name usually includes the active ingredient(s) of the product.
The non-proprietary name is sometimes called the generic name. Non-Proprietary Name What is the Non-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. Proprietary Name What is the Proprietary Name?
0 kommentar(er)
