NDC 76206-301 Lao Wei Wood Lock Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76206 - Rfx Pharmaceutical Co Ltd
- 76206-301 - Lao Wei Wood Lock Oil
Product Packages
NDC Code 76206-301-38
Package Description: 38 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 76206-301?
What are the uses for Lao Wei Wood Lock Oil?
Which are Lao Wei Wood Lock Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Lao Wei Wood Lock Oil 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:
- CLOVE OIL (UNII: 578389D6D0)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- CORYDALIS AMBIGUA TUBER (UNII: 1DN1EU584R)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- MYRRH (UNII: JC71GJ1F3L)
- DIPSACUS ASPER ROOT (UNII: LB1GQP4253)
- SPATHOLOBUS SUBERECTUS STEM (UNII: N51VZ363BA)
- PANAX NOTOGINSENG WHOLE (UNII: E7XOU43ESD)
- LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
What is the NDC to RxNorm Crosswalk for Lao Wei Wood Lock Oil?
- RxCUI: 1661791 - menthol 16 % / methyl salicylate 5 % Topical Oil
- RxCUI: 1661791 - menthol 160 MG/ML / methyl salicylate 50 MG/ML Topical Oil
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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".