NDC 58133-950 Relieveit Spraingo Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58133 - Cosmetic Specialty Labs, Inc.
- 58133-950 - Relieveit Spraingo Gel
Product Packages
NDC Code 58133-950-02
Package Description: 70 mL in 1 BOTTLE, PUMP
NDC Code 58133-950-16
Package Description: 474 mL in 1 BOTTLE, PUMP
NDC Code 58133-950-37
Package Description: 3780 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 58133-950?
What are the uses for Relieveit Spraingo Gel?
Which are Relieveit Spraingo Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
- SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
- SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP OIL (UNII: VDI0O08XRA)
- RUTA GRAVEOLENS FLOWERING TOP OIL (UNII: VDI0O08XRA) (Active Moiety)
Which are Relieveit Spraingo Gel 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:
- CYCLOMETHICONE (UNII: NMQ347994Z)
- METHYL ALCOHOL (UNII: Y4S76JWI15)
- GAULTHERIA PROCUMBENS LEAF (UNII: 2125M16OWN)
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 2165RE0K14)
- JUNIPER BERRY OIL (UNII: SZH16H44UY)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BENZOIN RESIN (UNII: GK21SBA74R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PROPYLENE GLYCOL 2-METHYLBUTYRATE (UNII: QH216IX8SV)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- CARBOMER 934 (UNII: Z135WT9208)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- SORBIC ACID (UNII: X045WJ989B)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- AMMONIUM LAURETH-7 SULFATE (UNII: 9LPV636QCV)
- KALANCHOE PINNATA LEAF (UNII: 3R963LO08T)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
* Please review the disclaimer below.
[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".