NDC 71309-105 Tension Headache Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71309 - Safrel Pharmaceuticals, Llc.
- 71309-105 - Tension Headache Relief
Product Characteristics
Product Packages
NDC Code 71309-105-02
Package Description: 200 CARTON in 1 BOTTLE / 1 BOTTLE in 1 CARTON (71309-105-24) / 24 TABLET, COATED in 1 BOTTLE
Product Details
What is NDC 71309-105?
What are the uses for Tension Headache Relief?
Which are Tension Headache Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Tension Headache Relief 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Tension Headache Relief?
- RxCUI: 307686 - acetaminophen 500 MG / caffeine 65 MG Oral Tablet
- RxCUI: 307686 - APAP 500 MG / Caffeine 65 MG Oral Tablet
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[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".