NDC 59779-191 Kids Pain Relief With Arnica
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-191 - Kids Pain Relief
Product Characteristics
Product Packages
NDC Code 59779-191-01
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 59779-191?
What are the uses for Kids Pain Relief With Arnica?
Which are Kids Pain Relief With Arnica UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
Which are Kids Pain Relief With Arnica 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:
- CARBOMER HOMOPOLYMER TYPE A (UNII: F68VH75CJC)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL COCOATE (UNII: WVK1CT5994)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PEG-20 GLYCERYL STEARATE (UNII: MJV0165YY8)
- PEG-100 STEARATE (UNII: YD01N1999R)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
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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".