NDC 61822-0045 Wu Yang Brand Medicated
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61822 - Guangzhou Baiyunshan Pharmaceutical Co., Ltd. Baiyunshan Hejigong Pharmaceutical Factory
- 61822-0045 - Wu Yang Brand Medicated
Product Packages
NDC Code 61822-0045-1
Package Description: 10 PLASTER in 1 BOX
NDC Code 61822-0045-2
Package Description: 1 PLASTER in 1 CAN
Product Details
What is NDC 61822-0045?
Which are Wu Yang Brand Medicated UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Wu Yang Brand Medicated 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:
- BLACK CATECHU (UNII: 55J167EEON)
- POLYGONUM CUSPIDATUM WHOLE (UNII: 1VDG5Y5HS6)
- TARAXACUM MONGOLICUM (UNII: 4E8QL88U6H)
- DAEMONOROPS DRACO RESIN (UNII: 787Z7N9UCU)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- MAMMAL BONE, FOSSILIZED (UNII: 0N1T3913DA)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- DIPSACUS ASPER ROOT (UNII: LB1GQP4253)
- MYRRH (UNII: JC71GJ1F3L)
What is the NDC to RxNorm Crosswalk for Wu Yang Brand Medicated?
- RxCUI: 1541608 - menthol 6 % / methyl salicylate 10 % Medicated Patch
- RxCUI: 1541608 - menthol 0.06 MG/MG / methyl salicylate 0.1 MG/MG Medicated Patch
* 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".