NDC 55614-640 Hong Hoa Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55614 - Madison One Acme Inc
- 55614-640 - Hong Hoa Pain Relieving
Product Packages
NDC Code 55614-640-02
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 55614-640?
Which are Hong Hoa Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Hong Hoa Pain Relieving 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:
- CINNAMON LEAF OIL (UNII: S92U8SQ71V)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- DRAGON'S BLOOD (UNII: M3YJ2C28IC)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
What is the NDC to RxNorm Crosswalk for Hong Hoa Pain Relieving?
- RxCUI: 2369408 - camphor 10 % / capsaicin 0.025 % / methyl salicylate 60 % Topical Oil
- RxCUI: 2369408 - camphor 0.1 MG/MG / capsaicin 0.00025 MG/MG / methyl salicylate 0.6 MG/MG 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".