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 16 of 44 · 874 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEBrookfield Pharmaceuticals, LLC.e824ba5b-3289-5ad4-e053-2995a90acc202025-11-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Walgreen Maximum strength pain relieving cleansingBENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDEWALGREENS CO.9a0443a2-f1a9-482d-b5ee-abe983e4ae322025-11-26WarningsExact identifier
unii: V13007Z41A
Walgreen Pain Relieving Fragrance FreeLIDOCAINE HYDROCHLORIDEWALGREENS CO.62c50ded-3fc9-4f65-9bfb-1144ed2e36b42025-11-26WarningsExact identifier
unii: V13007Z41A
WalgreensFIRST AID ANTISEPTICWalgreensae731d28-8530-4dd0-aef7-b25f784b47772025-11-26WarningsExact identifier
unii: V13007Z41A
Thermacare Heat Therapy Max Strength Lidocaine Pain Relief RollonTHERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF ROLLONClarion Brands LLC4482d34d-eaca-5522-e063-6394a90a6afb2025-11-26WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEA-S Medication Solutions82b377ee-0e3e-4cb9-a644-f45434c21cca2025-11-26Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
PUR-WASHWATERNiagara Pharmaceuticals Inc.beda35c3-9a8b-47ad-e053-2995a90a7b1b2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Thermacare Heat Therapy Max Strength Lidocaine Pain Relief GelTHERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GELClarion Brands LLC445db02a-c8e8-6ebb-e063-6294a90a43012025-11-24WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution42df73b0-20ee-d1aa-e063-6294a90aa2752025-11-21Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
JUST CBD RELIEF SOOTHINGLIDOCAINE HCLJust Brands LLCf9aff6e7-5702-f61c-e053-6294a90aa66f2025-11-17WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHenry Schein, Inc.313a7e1f-c1a9-4fa5-bb83-7256c271b3512025-11-17Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHenry Schein, Inc.335dfa50-56f3-4c02-b713-8eef4e28eb452025-11-17Warnings, Adverse reactionsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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