NDC 72581-428 Inmotion Pain Creme Ultra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72581 - Inmotion Products Llc
- 72581-428 - Inmotion Pain Creme Ultra Strength
Product Characteristics
Product Packages
NDC Code 72581-428-73
Package Description: 1 TUBE in 1 CARTON / 73 mL in 1 TUBE
Product Details
What is NDC 72581-428?
What are the uses for Inmotion Pain Creme Ultra Strength?
Which are Inmotion Pain Creme Ultra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Inmotion Pain Creme Ultra Strength 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:
- WATER (UNII: 059QF0KO0R)
- SESAME OIL (UNII: QX10HYY4QV)
- CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
- GLYCERIN (UNII: PDC6A3C0OX)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL LAURATE (UNII: Y98611C087)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SHEA BUTTER (UNII: K49155WL9Y)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALCOHOL (UNII: 3K9958V90M)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYL LAUROYL ARGINATE (UNII: E0K8J7A41B)
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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".