NDC 15667-5049 Pain Goodbye Medicated Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 15667 - Austin Biotechnology Inc
- 15667-5049 - Pain Goodbye Medicated Cream
Product Packages
NDC Code 15667-5049-4
Package Description: 280 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 15667-5049?
What are the uses for Pain Goodbye Medicated Cream?
Which are Pain Goodbye Medicated Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Pain Goodbye Medicated Cream 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:
- PEPPERMINT OIL (UNII: AV092KU4JH)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- JASMINE LACTONE (UNII: H8558L43SR)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CARBOMER 1342 (UNII: 809Y72KV36)
- CLOVE OIL (UNII: 578389D6D0)
What is the NDC to RxNorm Crosswalk for Pain Goodbye Medicated Cream?
- RxCUI: 1039690 - menthol 5 % Topical Cream
- RxCUI: 1039690 - menthol 50 MG/ML Topical Cream
- RxCUI: 1426260 - Pain Goodbye 5 % Topical Cream
- RxCUI: 1426260 - menthol 50 MG/ML Topical Cream [Pain Goodbye]
- RxCUI: 1426260 - Pain Goodbye 50 MG/ML Topical Cream
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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".