NDC 55264-005 Ginsenggo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55264 - Sinsin Pharmaceutical Co., Ltd.
- 55264-005 - Ginsenggo
Product Packages
NDC Code 55264-005-06
Package Description: 1 POUCH in 1 CARTON / 6 PATCH in 1 POUCH (55264-005-01)
Product Details
What is NDC 55264-005?
What are the uses for Ginsenggo?
Which are Ginsenggo UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- LEVOMENTHOL (UNII: BZ1R15MTK7) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Ginsenggo 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CASTOR OIL (UNII: D5340Y2I9G)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GELATIN (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- SILODRATE (UNII: 9T3UU8T0QK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- WATER (UNII: 059QF0KO0R)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- TARTARIC ACID (UNII: W4888I119H)
What is the NDC to RxNorm Crosswalk for Ginsenggo?
- RxCUI: 1486326 - camphor 0.7 % / levomenthol 1.4 % / methyl salicylate 2.8 % Medicated Patch
- RxCUI: 1486326 - camphor 0.007 MG/MG / levomenthol 0.014 MG/MG / methyl salicylate 0.028 MG/MG Medicated Patch
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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".