NDC 61291-011

Eugenol

Eugenol

Eugenol is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Polysciences, Inc. The primary component is Eugenol.

Product ID61291-011_0f0b6a1c-be77-40b6-b7be-2209f873891a
NDC61291-011
Product TypeHuman Otc Drug
Proprietary NameEugenol
Generic NameEugenol
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-01-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NamePolysciences, Inc
Substance NameEUGENOL
Active Ingredient Strength850 mg/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 61291-011-04

3.7 mL in 1 VIAL, GLASS (61291-011-04)
Marketing Start Date2015-01-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61291-011-04 [61291001104]

Eugenol LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-30
Marketing End Date2019-12-12

Drug Details

Active Ingredients

IngredientStrength
EUGENOL850 mg/mL

OpenFDA Data

SPL SET ID:138e7e95-0865-4b4d-bbdb-1e9700db4aa0
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 244327
  • NDC Crossover Matching brand name "Eugenol" or generic name "Eugenol"

    NDCBrand NameGeneric Name
    61291-011EugenolEugenol
    63083-1518EugenolEugenol
    27854-178AnaDent Childrens Kanka GelEugenol
    60630-566DenTek EugenolEugenol
    67659-400DenTek EugenolEugenol
    83062-400DenTek EugenolEugenol
    67659-415Eugenol Toothache MedicationEugenol
    10742-0009Red Cross Toothacheeugenol
    60630-608Walgreens Natural Eugenol/Toothache MedicationEugenol
    67659-405Walgreens Natural Eugenol/Toothache MedicationEugenol

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