1. Home
  2. Labeler Index
  3. Rinati Skin, Llc
  4. NDC Product Code: 76849-201 4rlf Topical Analgesic

NDC 76849-201 4rlf Topical Analgesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76849-201?
  4. 4rlf Topical Analgesic Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76849-201
Proprietary Name:
4rlf Topical Analgesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rinati Skin, Llc
Labeler Code:
76849
Product Label ID:
ee2832c7-6347-4c67-ac2b-579e6132afaa
Start Marketing Date: [9]
08-23-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76849-201-11

Package Description: 1 BLISTER PACK in 1 CARTON / 10 VIAL in 1 BLISTER PACK / 1 mL in 1 VIAL

Product Details

What is NDC 76849-201?

The NDC code 76849-201 is assigned by the FDA to the product 4rlf Topical Analgesic which is product labeled by Rinati Skin, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76849-201-11 1 blister pack in 1 carton / 10 vial in 1 blister pack / 1 ml in 1 vial. 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 4rlf Topical Analgesic?

■ Adults and children 2 years of age or older: Apply to the desired area and gently rub into the skin, not more than 3 to 4 times daily. ■ Children under the age of 2: Consult a physician.

Which are 4rlf Topical Analgesic UNII Codes?

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

Which are 4rlf Topical Analgesic 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:

* Please review the disclaimer below.

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".