NDC 72624-001 Chinese Medicine Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72624 - Hubei Lishizhen Modern Biological Medicine Group Co.,ltd.
- 72624-001 - Chinese Medicine Patch
Product Packages
NDC Code 72624-001-01
Package Description: 2 BAG in 1 BOX / 3 PACKAGE in 1 BAG / 240 mL in 1 PACKAGE
Product Details
What is NDC 72624-001?
What are the uses for Chinese Medicine Patch?
Which are Chinese Medicine Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (Active Moiety)
Which are Chinese Medicine Patch 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:
- WATER (UNII: 059QF0KO0R)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
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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".