NDC 13107-075 Butalbital, Acetaminophen And Caffeine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13107 - Aurolife Pharma, Llc
- 13107-075 - Butalbital, Acetaminophen And Caffeine
Product Characteristics
Product Packages
NDC Code 13107-075-05
Package Description: 500 CAPSULE in 1 BOTTLE
NDC Code 13107-075-30
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 13107-075?
What are the uses for Butalbital, Acetaminophen And Caffeine?
Which are Butalbital, Acetaminophen And Caffeine UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUTALBITAL (UNII: KHS0AZ4JVK)
- BUTALBITAL (UNII: KHS0AZ4JVK) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Butalbital, Acetaminophen And Caffeine Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN (UNII: 2G86QN327L)
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE (UNII: FZ989GH94E)
- CROSPOVIDONE (UNII: 68401960MK)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SHELLAC (UNII: 46N107B71O)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Butalbital, Acetaminophen And Caffeine?
- RxCUI: 238153 - butalbital 50 MG / acetaminophen 325 MG / caffeine 40 MG Oral Capsule
- RxCUI: 238153 - acetaminophen 325 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule
- RxCUI: 238153 - APAP 325 MG / butalbital 50 MG / Caffeine 40 MG Oral Capsule
* Please review the disclaimer below.
Patient Education
Acetaminophen, Butalbital, and Caffeine
This combination of drugs is used to relieve tension headaches. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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Pain Relievers
Pain relievers are medicines that reduce or relieve headaches, sore muscles, arthritis, or other aches and pains. There are many different pain medicines, and each one has advantages and risks. Some types of pain respond better to certain medicines than others. Each person may also have a slightly different response to a pain reliever.
Over-the-counter (OTC) medicines are good for many types of pain. There are two main types of OTC pain medicines: acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs (NSAIDs). Aspirin, naproxen (Aleve), and ibuprofen (Advil, Motrin) are examples of OTC NSAIDs.
If OTC medicines don't relieve your pain, your doctor may prescribe something stronger. Many NSAIDs are also available at higher prescription doses. The most powerful pain relievers are opioids. They are very effective, but they can sometimes have serious side effects. There is also a risk of addiction. Because of the risks, you must use them only under a doctor's supervision.
There are many things you can do to help ease pain. Pain relievers are just one part of a pain treatment plan.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".