NDC 55277-1001 Pancold S
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55277 - Kafus Co., Ltd
- 55277-1001 - Pancold S
Product Packages
NDC Code 55277-1001-1
Package Description: 30 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 55277-1001?
What are the uses for Pancold S?
Which are Pancold S UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
- METHYLEPHEDRINE HYDROCHLORIDE, DL- (UNII: 99214P83XM)
- METHYLEPHEDRINE, DL- (UNII: SHS9PGQ2LS) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Pancold S 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:
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- LEMON (UNII: 24RS0A988O)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U)
- ORANGE (UNII: 5EVU04N5QU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Pancold S?
- RxCUI: 1366508 - acetaminophen 10 MG/ML / caffeine 1 MG/ML / chlorpheniramine maleate 0.083 MG/ML / guaifenesin 2.78 MG/ML / methylephedrine hydrochloride, DL- 0.583 MG/ML Oral Solution
- RxCUI: 1366508 - APAP 10 MG/ML / Caffeine 1 MG/ML / Chlorpheniramine Maleate 0.083 MG/ML / Guaifenesin 2.78 MG/ML / METHYLEPHEDRINE HYDROCHLORIDE, DL- 0.583 MG/ML Oral Solution
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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".