FDA.reportPublic FDA data

NDC 68229-200-01 - Alocane

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
68229-200
Requested NDC
68229-200-01
Package NDCs from labels
68229-200-01, 68229-200-02
Manufacturer
Quest Products, Inc. | Fill Tech USA
Effective date
2013-06-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Alocane - Quest Products, Inc. | Fill Tech USAQuest Products, Inc. | Fill Tech USA2013-06-14HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68229-200-022022-02-25C16284748780-19d75b9d0-fa6c-f424-e053-dadaa90a57ceAlocane ®
68229-200-022020-01-31C16284748780-19d75b9d0-fa6c-f424-e053-dadaa90a57ceAlocane ®

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68229-200-02ML - Milliliter68229-200f4837df7-1556-4272-809d-9dcd8c0f7bbe12017-09-11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Lidocaine HydrochlorideACTIVE INGREDIENTV13007Z41AALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
LidocaineACTIVE MOIETY98PI200987ALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
.Alpha.-Tocopherol AcetateINACTIVE INGREDIENT9E8X80D2L0ALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0XALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
Caprylyl GlycolINACTIVE INGREDIENT00YIU5438UALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
ChlorphenesinINACTIVE INGREDIENTI670DAL4SZALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
Dimethyl IsosorbideINACTIVE INGREDIENTSA6A6V432SALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
Hydroxyethyl Cellulose (5500 MPA.S at 2%)INACTIVE INGREDIENTM825OX60H9ALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
PhenoxyethanolINACTIVE INGREDIENTHIE492ZZ3TALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
PropanediolINACTIVE INGREDIENT5965N8W85TALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RALOCANE (LIDOCAINE HYDROCHLORIDE) OINTMENT [QUEST PRODUCTS, INC.]1

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 42 of 44 · 863 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERFresenius Kabi USA, LLCb45e9f1d-9c48-4b46-8541-d846b89540df2022-10-26Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye washPURIFIED WATERMcKessonbd089fde-24ba-4de5-e053-2995a90a39bb2022-10-18WarningsExact identifier
unii: 059QF0KO0R
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.fecd1797-7757-4da8-b3a1-24b2586342432022-10-12Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.8ae0656c-36fb-48fb-886b-1031d11da5522022-10-12Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.deec52c7-ebcf-422e-beab-bc1df2fe30cb2022-10-12Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Bach Original Flower Remedies Rock WaterWATERNelson Bach USA Limitedea242559-1618-3354-e053-2a95a90a1a952022-10-03WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERMedical Purchasing Solutions, LLCe90b47e3-9636-b9ee-e053-2a95a90ad48c2022-09-19Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
LidotranLIDOCAINE HYDROCHLORIDEPureTek Corporationcf715e54-c413-1e8f-e053-2995a90a076d2022-09-19Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LidotholLIDOCAINE HCL, MENTHOLAsclemed USA, Inc.6d7adaca-67dd-4a4b-a85c-d1c2a568dee22022-09-09Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Sterile WaterWATERFresenius Kabi USA, LLCf42ac50f-0ec5-4713-a4c8-99d972d90bed2022-06-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCe71c6c83-d518-496c-b2ab-efd5987e47832022-06-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Miracle FootCream LavenderUREA, GLYCERIN, ALOE, DISODIUM EDTAAloe Vera Korea Co.,Ltd.db520c80-2a2a-5eb1-e053-2995a90a5bb42022-03-28WarningsExact identifier
unii: ZY81Z83H0X
Miracle FootCream LemonUREA, GLYCERIN, ALOE, DISODIUM EDTAAloe Vera Korea Co.,Ltd.db525c63-29fd-2033-e053-2995a90a56b92022-03-28WarningsExact identifier
unii: ZY81Z83H0X
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDENovitium Pharma LLCffb2d794-2c88-48a2-beff-d01b6fcea51f2022-03-25Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lydexa 4.12%LIDOCAINE HYDROCHLORIDEPureTek Corporationaa1c9d39-1283-8c6b-e053-2a95a90af5b52022-03-02Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
d8db9210-d732-b9e4-e053-2a95a90a79fec08e418e-12a8-44c7-b448-7b1514a89f332022-02-25WarningsExact identifier
spl set id: c08e418e-12a8-44c7-b448-7b1514a89f33
Sterile WaterWATERAmerican Regent, Inc.78b35864-4bbc-4759-a5c1-7e4f25e229322022-01-31Boxed warningExact identifier
unii: 059QF0KO0R
TreprostinilTREPROSTINILDr.Reddy's Laboratories Inc.,33050ee2-519b-1f0b-d4df-9e14dd329c572021-12-23Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEInternational Medication Systems, Limited2c48cfac-81eb-4a81-8590-bc94574dd4c32021-12-14Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Sterile WaterSTERILE WATERB. Braun Medical Inc.d99f9133-e4d0-4dee-b611-dbc3f918b5472021-08-09Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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