NDC 42217-206 Pain Relief Tincture
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 42217-206?
What are the uses for Pain Relief Tincture?
Which are Pain Relief Tincture UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Pain Relief Tincture 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:
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- ZANTHOXYLUM PIPERITUM WHOLE (UNII: Y8IKP41338)
- KAEMPFERIA GALANGA WHOLE (UNII: NU6Y8418BH)
- CINNAMON (UNII: 5S29HWU6QB)
- GREEN PEPPERCORN (UNII: 6G53L8ESRK)
- CHINESE RHUBARB ROOT (UNII: 5U759027OH)
- LONG PEPPER (UNII: 2NMG4EA7B1)
- GINGER (UNII: C5529G5JPQ)
- CLOVE (UNII: K48IKT5321)
- BORNEOL (UNII: M89NIB437X)
- ETHANOL, 2-(BIS(2-METHYLPROPYL)PHENOXY)- (UNII: AUK0O5KW1Y)
What is the NDC to RxNorm Crosswalk for Pain Relief Tincture?
- RxCUI: 1606183 - camphor 5 % / menthol 1.3 % Topical Solution
- RxCUI: 1606183 - camphor 50 MG/ML / menthol 13 MG/ML Topical Solution
- RxCUI: 1606183 - camphor 5 % / menthol 1.3 % Topical Tincture
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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".