76849-201 NDC - 4RLF TOPICAL ANALGESIC ()

Drug Information

Product NDC: 76849-201

Proprietary Name: 4RLF Topical Analgesic

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rinati Skin, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/23/2021

Package Information

No. Package Code Package Description Billing Unit
176849-201-111 BLISTER PACK in 1 CARTON (76849-201-11) / 10 VIAL in 1 BLISTER PACK / 1 mL in 1 VIAL

NDC Record

Field Name Field Value Definition
PRODUCT NDC76849-201The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME4RLF Topical AnalgesicThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/23/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERinati Skin, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024