NDC 17856-0138-01 - Lidocaine hydrochloride

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
17856-0138
Requested NDC
17856-0138-01
Package NDCs from labels
17856-0138-3, 17856-0138-1, 17856-0138-4, 17856-0138-2, 17856-0138-6, 17856-0138-5, 17856-0138-01
Manufacturer
ATLANTIC BIOLOGICALS CORP.
Effective date
2025-05-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lidocaine Hydrochloride Oral Topical Solution USP, 2% (Viscous)ATLANTIC BIOLOGICALS CORP.2025-05-12HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-0138-1Lidocaine hydrochloride50 in 1 BOX, UNIT-DOSESOLUTION503
17856-0138-2Lidocaine hydrochloride50 in 1 BOX, UNIT-DOSESOLUTION503
17856-0138-3Lidocaine hydrochloride15 mL in 1 CUP, UNIT-DOSESOLUTION153
17856-0138-4Lidocaine hydrochloride20 mL in 1 CUP, UNIT-DOSESOLUTION203
17856-0138-5Lidocaine hydrochloride72 in 1 BOX, UNIT-DOSESOLUTION723
17856-0138-6Lidocaine hydrochloride5 mL in 1 CUP, UNIT-DOSESOLUTION53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0138LIDOCAINE HYDROCHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.]3Current NDC, 6 package rows20250514_75d17334-6876-42d0-8a02-82669d139e4f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-0138-1ML - Milliliter17856-0138c494c261-df59-4696-919e-e062bcc63ab612024-03-12
17856-0138-2ML - Milliliter17856-0138c72c7dce-4880-4309-b60c-c5d0f465dce512024-03-12

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 26 of 47 · 931 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LidocaineLIDOCAINE HYDROCHLORIDEFresenius Kabi USA, LLCcddb2b22-fce3-8967-6e54-dca3df5ac4b32025-03-26Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEPreferred Pharmaceuticals Inc.abf60c5c-66df-4894-aa8f-bf770a6e9d002025-03-24Warnings, Adverse reactionsExact identifier
rxcui: 1010739
unii: V13007Z41A
Lignospan StandardLIDOCAINE HYDROCHLORIDE AND EPINEPHRINESeptodont, Inc.f902d2b4-28fc-41b1-a9f7-0d1a63c598aa2025-03-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lignospan ForteLIDOCAINE HYDROCHLORIDE AND EPINEPHRINESeptodont, Inc.f8ca7d03-01c8-450f-9279-59789c3497ea2025-03-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDENuCare Pharmaceuticals,Inc.037764d3-da0e-5ebb-e063-6294a90ab6e02025-03-19Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA216780
rxcui: 1010739
unii: V13007Z41A
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: Z8IX2SC1OH
unii: A2I8C7HI9T
LidocaineLIDOCAINE HYDROCHLORIDEARMAS PHARMACEUTICALS INC.2f6e0f3d-ceaf-a853-e063-6394a90a8efb2025-03-07Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
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: V13007Z41A
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
Lightning Products BURN RELIEFLIDOCAINE HYDROCHLORIDENantong Health & Beyond Hygienic Products Inc.555ac696-e761-4a5a-bed8-945dc64d5be52025-02-27WarningsExact identifier
unii: V13007Z41A
AeroWash EyewashEYEWASH SOLUTIONAero Healthcare US LLCa477de08-4301-0ee5-e053-2995a90af79d2025-02-26WarningsExact identifier
unii: 059QF0KO0R
LidoPro Pain ReliefCAPSAICIN AND LIDOCAINEPreferred Pharmaceuticals Inc.c259ef92-5d07-4590-adf1-3a106333eee02025-02-21WarningsExact identifier
unii: V13007Z41A
LidocaineLIDOCAINE HYDROCHLORIDEFresenius Kabi USA, LLCf1b26274-a55e-4321-b96c-ce0df830f2052025-02-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEMcKesson Corporation dba SKY Packaginge1eabd6b-9bb8-646f-e053-2a95a90a7b832025-02-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Sunburn Relief GelLIDOCAINE HCLJell Pharmaceuticals Pvt. Ltd2e7c49de-5438-4858-e063-6294a90ad98c2025-02-19WarningsExact identifier
unii: V13007Z41A
CANNA NUMB Roll OnLIDOCAINE HYDROCHLORIDE, MENTHOLCannanumb LLCc1eb0348-3b0e-4f1c-a46b-1ff4aa165fb42025-02-17WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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