FDA.reportPublic FDA data

NDC 27102-806 - PETCO

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
27102-806
Package NDCs from labels
27102-806-07
Manufacturer
PETCO | United Pet Group | JUNGLE LABORATORIES CORPORATION
Effective date
2010-03-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PETCO - PETCO | United Pet Group | JUNGLE LABORATORIES CORPORATIONPETCO | United Pet Group | JUNGLE LABORATORIES CORPORATION2010-03-02OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
27102-806-07PETCO236 g in 1 BOTTLE, SPRAYLIQUID2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
27102-806PETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]31 package rows20100727_27d9340c-2e17-462e-805b-cff348efa041.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41APETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
LIDOCAINEACTIVE MOIETY98PI200987PETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
ALLANTOININACTIVE INGREDIENT344S277G0ZPETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XPETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W7PETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
DENATONIUM BENZOATEINACTIVE INGREDIENT4YK5Z54AT2PETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
GLYCERININACTIVE INGREDIENTPDC6A3C0OXPETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3
WaterINACTIVE INGREDIENT059QF0KO0RPETCO (LIDOCAINE HYDROCHLORIDE) LIQUID [PETCO]3

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 70 of 113 · 2,244 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LESONEL FEMININE FOAMING WASHALLANTOINACE PHARMACEUTICAL CO.,LTD.3033b1b3-21b7-9b5b-e063-6294a90a54c52025-03-13WarningsExact identifier
unii: 344S277G0Z
XeroBurn Burn GelLIDOCAINE HYDROCHLORIDEDynarex Corporation58985046-ca9c-12be-e053-2991aa0abe722025-03-13WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDENovagenix Labs LLC7567ffb5-953a-4be9-9a02-c5a50dcd93062025-03-12Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
AddiclenzASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, BETA VULGARIS, BISPHENOL A, BOLDO, CHELIDONIUM MAJUS, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PETROSELINUM SATIVUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, TARAXACUM OFFICINALE, ZINCUM METALLICUMDeseret Biologicals, Inc.25036c26-1c21-4e5a-b4db-b8e1774583412025-03-11WarningsExact identifier
unii: F5UM2KM3W7
Antimicrobial Foaming HandBENZALKONIUM CHLORIDEHealth Technology Professional Products, Incdbca0970-88ca-04a4-e053-2995a90a68f22025-03-07WarningsExact identifier
unii: F5UM2KM3W7
LidocaineLIDOCAINE HYDROCHLORIDEARMAS PHARMACEUTICALS INC.2f6e0f3d-ceaf-a853-e063-6394a90a8efb2025-03-07Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Moxie Hand WipesBENZALKONIUM CHLORIDESkaffles Group17cd6c1a-7b31-3975-e063-6294a90a41c52025-03-07WarningsExact identifier
unii: F5UM2KM3W7
Curist Hemorrhoid Fissure ReliefLIDOCAINELittle Pharma, Inc2fb02b00-acdb-5184-e063-6294a90ae1c82025-03-06WarningsExact identifier
unii: PDC6A3C0OX
XTRABENZALKONIUM CHLORIDEZhejiang Jifu Daily Chemical Co., Ltd.27df3fce-3958-d4ea-e063-6394a90a17852025-03-06WarningsExact identifier
unii: F5UM2KM3W7
XTRABENZALKONIUM CHLORIDEMY IMPORTS USA LLC27f4ff15-5480-8842-e063-6294a90ad35b2025-03-06WarningsExact identifier
unii: F5UM2KM3W7
Redicare Burn GelREDICARE BURN GELRedicare LLC947ac362-acfb-3508-e053-2a95a90a28732025-03-05WarningsExact identifier
unii: V13007Z41A
Thera Plus Pain Relief CleansingBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEFourstar Group USA, Inc.513a620e-f69a-488d-8abc-36e2efccdc132025-03-04WarningsExact identifier
unii: F5UM2KM3W7
unii: V13007Z41A
Thera Plus HemorrhoidalGLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDEFOURSTAR GROUP USA, INC.87143a7a-7b2d-4b67-afda-2355697e73002025-03-04WarningsExact identifier
unii: PDC6A3C0OX
Ben E. Keith FIHSBENZALKONIUM CHLORIDEBen E. Keith Foods4ca21370-1ecf-42c6-9c32-79cf994c336b2025-03-03WarningsExact identifier
unii: F5UM2KM3W7
Algonquin HanClean FoamBENZALKONIUM CHLORIDEWhisk Products, Inc.2f73c3a7-426e-51f4-e063-6394a90aad4f2025-03-03WarningsExact identifier
unii: F5UM2KM3W7
4% lidocaine plus 1% menthol Pain Relief PatchPAIN RELIEF PATCH, PAIN RELIEF STRIPXuzhou Lanting Pharmaceutical Co., Ltd2f98ee5e-e4eb-fbda-e063-6394a90a709c2025-03-01WarningsExact identifier
unii: V13007Z41A
4% Lidocaine Pain Relief PatchLIDOCAINE PAIN RELIEF PATCHXuzhou Lanting Pharmaceutical Co., Ltd2f98a6e9-b7c4-061e-e063-6294a90a67282025-03-01WarningsExact identifier
unii: V13007Z41A
YVTYVT NONI AMPOULE FACIAL SERUMMORINDA CITRIFOLIA FRUIT,ALLANTOIN,MELIA AZADIRACHTA LEAF,ADENOSINEBeijing JUNGE Technology Co., Ltd.2f3f2a14-d030-12e7-e063-6294a90ab8892025-02-28WarningsExact identifier
unii: 344S277G0Z
YVTYVT COPPER PEPTIDES FACIAL SERUMBETAINE,COPPER TRIPEPTIDE-1,ALLANTOIN,CHRYSANTHELLUM INDICUM WHOLEBeijing JUNGE Technology Co., Ltd.2f406a3e-906c-cba3-e063-6394a90aadd02025-02-28WarningsExact identifier
unii: 344S277G0Z
Lightning Products BURN RELIEFLIDOCAINE HYDROCHLORIDENantong Health & Beyond Hygienic Products Inc.555ac696-e761-4a5a-bed8-945dc64d5be52025-02-27WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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