NDC 29500-2433 Muscle Rub Ultra Strength Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 29500 - Personal Care Products, Inc.
- 29500-2433 - Muscle Rub
Product Packages
NDC Code 29500-2433-1
Package Description: 42 g in 1 TUBE
Product Details
What is NDC 29500-2433?
What are the uses for Muscle Rub Ultra Strength Pain Relieving?
Which are Muscle Rub Ultra Strength Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Muscle Rub Ultra Strength 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:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
What is the NDC to RxNorm Crosswalk for Muscle Rub Ultra Strength Pain Relieving?
- RxCUI: 1291226 - menthol 2.5 % Topical Cream
- RxCUI: 1291226 - menthol 25 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".