NDC 58133-950 Relieveit Spraingo Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
58133-950
Proprietary Name:
Relieveit Spraingo Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cosmetic Specialty Labs, Inc.
Labeler Code:
58133
Start Marketing Date: [9]
10-17-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 58133-950 is assigned by the FDA to the product Relieveit Spraingo Gel which is product labeled by Cosmetic Specialty Labs, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 58133-950-02 70 ml in 1 bottle, pump , 58133-950-16 474 ml in 1 bottle, pump , 58133-950-37 3780 ml in 1 bottle, pump . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Relieveit Spraingo Gel?

Adults and children 2 years and over:Shake well before using •Apply a sufficientamount of RelieveIt® SprainGo Gel to cover theaffected area • Repeat as needed • Afterapplying, wash hands with soap and waterChildren under 2: consult a doctor

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:

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Product Footnotes

[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".