NDC 69151-100 Aspi-rub Pain Reliever
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69151 - Aspirub Enterprises Llc
- 69151-100 - Aspi-rub
Product Packages
NDC Code 69151-100-01
Package Description: 59 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69151-100?
What are the uses for Aspi-rub Pain Reliever?
Which are Aspi-rub Pain Reliever UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Aspi-rub Pain Reliever 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:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- CASTOR OIL (UNII: D5340Y2I9G)
- WHITE PINE OIL (UNII: HA5CX6676U)
- GLYCERIN (UNII: PDC6A3C0OX)
- MENTHOL (UNII: L7T10EIP3A)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Aspi-rub Pain Reliever?
- RxCUI: 1549154 - methyl salicylate 23 % Topical Spray
- RxCUI: 1549154 - methyl salicylate 230 MG/ML Topical Spray
- RxCUI: 1549159 - Aspi-Rub Pain Reliever 23 % Topical Spray
- RxCUI: 1549159 - methyl salicylate 230 MG/ML Topical Spray [Aspi-Rub]
- RxCUI: 1549159 - Aspi-Rub 230 MG/ML Topical Spray
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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".