NDC 66051-011

Haws Personal Emergency Eyewash - DUO Saline

Water

Haws Personal Emergency Eyewash - DUO Saline is a Ophthalmic Liquid in the Human Otc Drug category. It is labeled and distributed by Haws Corporation. The primary component is Water.

Product ID66051-011_a08351ae-5124-40f4-8651-fdb521cb9acd
NDC66051-011
Product TypeHuman Otc Drug
Proprietary NameHaws Personal Emergency Eyewash - DUO Saline
Generic NameWater
Dosage FormLiquid
Route of AdministrationOPHTHALMIC
Marketing Start Date2016-06-23
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart349
Labeler NameHaws Corporation
Substance NameWATER
Active Ingredient Strength99 mL/100mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 66051-011-34

1000 mL in 1 BOTTLE (66051-011-34)
Marketing Start Date2016-06-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66051-011-34 [66051001134]

Haws Personal Emergency Eyewash - DUO Saline LIQUID
Marketing CategoryOTC monograph final
Application Numberpart349
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-23
Marketing End Date2018-10-31

Drug Details

Active Ingredients

IngredientStrength
WATER99.1 mL/100mL

OpenFDA Data

SPL SET ID:fefca6de-3057-48a4-bec7-ea211793a9cd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1053429
  • NDC Crossover Matching brand name "Haws Personal Emergency Eyewash - DUO Saline" or generic name "Water"

    NDCBrand NameGeneric Name
    66051-011Haws Personal Emergency Eyewash - DUO SalineHaws Personal Emergency Eyewash - DUO Saline
    0404-9970Bacteriostatic WaterWater
    0173-0518Diluentwater
    0173-0857Diluentwater
    0404-7198EyewashWater
    0264-2101Sterile WaterWater
    0264-7385Sterile WaterWater
    0264-7850Sterile WaterWater
    0338-0003Sterile WaterWater
    0338-0004Sterile WaterWater
    0338-0013Sterile WaterWater
    0404-9959Sterile WaterWater
    0404-9971STERILE WATERWATER
    0409-4887Sterile WaterWATER

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.