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Drug Information

Product NDC: 24208-537

Proprietary Name: LUMIFY Redness Reliever Eye Drops


Active Ingredient(s):

Administration Route(s): OPHTHALMIC

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • Adrenergic alpha-Agonists [MoA];
  • alpha-Adrenergic Agonist [EPC]

Labeler Information

Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA208144
Marketing Category: NDA
Start Marketing Date:12/22/2017

Package Information

No. Package Code Package Description Billing Unit
124208-537-011 AMPULE in 1 CARTON (24208-537-01) / .4 mL in 1 AMPULE
224208-537-051 BOTTLE, DROPPER in 1 CARTON (24208-537-05) / 5 mL in 1 BOTTLE, DROPPER
324208-537-081 BOTTLE, DROPPER in 1 CARTON (24208-537-08) / 2.5 mL in 1 BOTTLE, DROPPERML
424208-537-101 AMPULE in 1 CARTON (24208-537-10) / .4 mL in 1 AMPULE
524208-537-152 BOTTLE, DROPPER in 1 CARTON (24208-537-15) / 7.5 mL in 1 BOTTLE, DROPPER
624208-537-251 BOTTLE, DROPPER in 1 CARTON (24208-537-25) / 7.5 mL in 1 BOTTLE, DROPPERML
724208-537-751 BOTTLE, DROPPER in 1 CARTON (24208-537-75) / 7.5 mL in 1 BOTTLE, DROPPER
824208-537-991 BOTTLE, DROPPER in 1 CARTON (24208-537-99) / 2.5 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC24208-537The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELUMIFY Redness Reliever Eye DropsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBRIMONIDINE TARTRATEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEOPHTHALMICThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/22/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at under Structured Product Labeling Resources.
APPLICATION NUMBERNDA208144This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEBausch & Lomb IncorporatedName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBRIMONIDINE TARTRATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PHARM CLASSESAdrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] 

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This page was last updated on: 2/1/2023