59276-209 NDC - A-MED BRAND FIRST AID EYE AND SKIN-RINSE (PURIFIED WATER)

Drug Information

Product NDC: 59276-209

Proprietary Name: A-Med brand First Aid Eye and Skin-Rinse

Non Proprietary Name: Purified Water

Active Ingredient(s):
  • 98.577 mL/100mL WATER


Administration Route(s): OPHTHALMIC

Dosage Form(s): SOLUTION

Labeler Information

Labeler Name: Oliver Landon Intl Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:11/1/2013

Package Information

No. Package Code Package Description Billing Unit
159276-209-1015 mL in 1 VIAL (59276-209-10)
259276-209-125 VIAL in 1 BOX (59276-209-12) / 15 mL in 1 VIAL
359276-209-224 VIAL in 1 BOX (59276-209-22) / 15 mL in 1 VIAL
459276-209-3030 mL in 1 VIAL, SINGLE-USE (59276-209-30)
559276-209-40118 mL in 1 BOTTLE, PLASTIC (59276-209-40)
659276-209-50148 mL in 1 BOTTLE, PLASTIC (59276-209-50)
759276-209-60236 mL in 1 BOTTLE, PLASTIC (59276-209-60)
859276-209-70350 mL in 1 BOTTLE, DISPENSING (59276-209-70)
959276-209-80474 mL in 1 BOTTLE, PLASTIC (59276-209-80)
1059276-209-90947 mL in 1 BOTTLE, PLASTIC (59276-209-90)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59276-209The 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 NAMEA-Med brand First Aid Eye and Skin-RinseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPurified WaterThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe 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 DATE11/1/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct 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 www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart349This 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 NAMEOliver Landon Intl Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEWATERAn 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.
ACTIVE NUMERATOR STRENGTH98.577 
ACTIVE INGRED UNITmL/100mL 

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