NDC 70486-100 Chi-myst Synergy Topical

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:
70486-100
Proprietary Name:
Chi-myst Synergy Topical
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prescription Care Llc
Labeler Code:
70486
Start Marketing Date: [9]
06-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70486-100-00

Package Description: 100 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 70486-100?

The NDC code 70486-100 is assigned by the FDA to the product Chi-myst Synergy Topical which is product labeled by Prescription Care Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70486-100-00 100 ml in 1 bottle, spray . 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.

Which are Chi-myst Synergy Topical UNII Codes?

The UNII codes for the active ingredients in this product are:

  • BUPIVACAINE HYDROCHLORIDE (UNII: 7TQO7W3VT8)
  • BUPIVACAINE (UNII: Y8335394RO) (Active Moiety)
  • KETOROLAC TROMETHAMINE (UNII: 4EVE5946BQ)
  • KETOROLAC (UNII: YZI5105V0L) (Active Moiety)
  • CHITOSAN LOW MOLECULAR WEIGHT (20-200 MPA.S) (UNII: SBD1A2I75N)
  • CHITOSAN LOW MOLECULAR WEIGHT (20-200 MPA.S) (UNII: SBD1A2I75N) (Active Moiety)
  • LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
  • LIDOCAINE (UNII: 98PI200987) (Active Moiety)

Which are Chi-myst Synergy Topical 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".