FDA.reportPublic FDA data

NDC 51437-202 - Medicated Anti-Itch

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51437-202
Package NDCs from labels
51437-202-08
Manufacturer
Nootie, LLC
Effective date
2016-08-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Medicated Anti-Itch - Nootie, LLCNootie, LLC2016-08-16OTC ANIMAL DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 47 of 47 · 934 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CuadridermaBACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDEProMex LLC4fa99b96-ab4b-4523-82bc-343dbaf39fb62022-01-25WarningsExact identifier
unii: 88AYB867L5
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEInternational Medication Systems, Limited2c48cfac-81eb-4a81-8590-bc94574dd4c32021-12-14Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Bactine MaxBENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDEWellSpring Pharmaceutical Corporation28e8a311-20a4-45a1-8d5d-ca42b101c2752021-02-24WarningsExact identifier
unii: V13007Z41A
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDEWestminster Pharmaceuticals, LLC6702589d-6a15-40fe-877a-a9a1a4ad0f7a2020-11-30Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDEProficient Rx LP5b4b36dd-da60-47de-a2c1-517a52ab35492020-05-01Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.b8803e38-fe30-48ec-9399-013f2880e0eb2020-04-09Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
DermacinRx LidotralLIDOCAINE HYDROCHLORIDEPureTek Corporation23efec58-67cc-418d-85f5-7ef156443cbf2019-02-04Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
EhaLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.09835640-55c3-4bfa-9ad3-15d37f06e8712018-11-01WarningsExact identifier
unii: V13007Z41A
SunBurnt PLUS Pain ReliefLIDOCAINE HYDROCHLORIDEWelmedix LLC dba Welmedix Consumer Healthcare6363c695-f801-407d-a4e1-b0d9cfa0a2732018-03-13WarningsExact identifier
unii: V13007Z41A
UnburnLIDOCAINE HYDROCHLORIDEWater-Jel Technologies0c504ba8-8a40-43dd-8c68-62ed106b32a22017-12-01WarningsExact identifier
unii: V13007Z41A
UnburnLIDOCAINE HYDROCHLORIDEWater-Jel Technologies40164231-1556-4714-9e27-9d41e3c714472017-11-30WarningsExact identifier
unii: V13007Z41A
First Aid BurnBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEWater-Jel Technologies25ebf112-8ac3-4402-9a87-00e454ab7efa2017-11-30WarningsExact identifier
unii: V13007Z41A
First Degree Maximum Strength BurnPRAMOXINE HYDROCHLORIDEWelmedix LLC1afa337e-f411-42df-b2f5-5f72c9b52ffa2017-03-09WarningsExact identifier
unii: 88AYB867L5
CVS Pain Relieving First Aid AntisepticLIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDECVS Pharmacy454b1773-eda8-5610-e054-00144ff88e882017-01-04WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.