NDC 63323-486-01 - Xylocaine
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
- 63323-486
- Requested NDC
- 63323-486-01
- Package NDCs from labels
- 63323-486-41, 63323-486-26, 63323-486-01, 63323-486-17, 63323-486-02, 63323-486-27, 63323-486-05, 63323-486-57
- Manufacturer
- Sportpharm LLC
- Effective date
- 2026-02-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Xylocaine - Sportpharm LLC | Sportpharm LLC | 2026-02-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine 2% (lidocaine HCl, injection, USP) 20mg/mL 50mL Multiple dose vial | Henry Schein, Inc. | 2025-11-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine - ASCLEMED USA INC | ASCLEMED USA INC. DBA ENOVACHEM | ASCLEMED USA INC | ASCLEMED USA INC. DBA ENOVACHEM | 2025-06-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-05-31 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine MPF - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2025-04-22 | HUMAN PRESCRIPTION DRUG LABEL |
| XYLOCAINE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-01-27 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine - General Injectables & Vaccines, Inc | General Injectables & Vaccines, Inc | 2022-12-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine MPF - Fresenius Kabi USA, LLC | Fresenius Kabi Austria | Fresenius Kabi USA, LLC | Fresenius Kabi Austria | 2021-08-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine MPF - Cardinal Health | Cardinal Health | 2019-09-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine | REMEDYREPACK INC. | 2019-04-30 | HUMAN PRESCRIPTION DRUG LABEL |
| Xylocaine | REMEDYREPACK INC. | 2019-02-12 | HUMAN PRESCRIPTION DRUG LABEL |
| General Surgery Kit - Centurion Medical Products | APP Pharmaceuticals, LLC | Centurion Medical Products | APP Pharmaceuticals, LLC | 2013-10-02 | MEDICAL DEVICE |
| Xylocaine - Centurion Medical Products | APP Pharmaceuticals, LLC | Centurion Medical Products | APP Pharmaceuticals, LLC | 2012-03-15 | MEDICAL DEVICE |
| Xylocaine | Physicians Total Care, Inc. | 2012-02-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63323-486-01 | Xylocaine | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | 13 | |
| 63323-486-02 | Xylocaine | 20 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 20 | 13 | |
| 63323-486-05 | Xylocaine | 50 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 50 | 13 | |
| 63323-486-17 | Xylocaine | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 13 | |
| 63323-486-27 | Xylocaine | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 13 | |
| 63323-486-57 | Xylocaine | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 13 | |
| 63323-486-26 | Xylocaine | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 7 | |
| 63323-486-41 | Xylocaine | 20 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 20 | 7 | |
| 63323-486-17 | Cardiovascular Procedure Kit | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 mL | 20 mg in 1mL | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63323-486 | XYLOCAINE MPF (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION XYLOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION XYLOCAINE MPF (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] | 13 | Current NDC, Legacy NDC, 6 package rows | 20210831_ba082c2f-64f4-419d-9c88-74f203316e17.zip |
| 63323-486 | XYLOCAINE MPF (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION XYLOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20250515_4dd52202-8eef-4136-92dd-ada573b7cf74.zip |
| 63323-486 | CARDIOVASCULAR PROCEDURE KIT () KIT [CENTURION MEDICAL PRODUCTS] | 1 | Current NDC, Legacy NDC | 20120316_eed8f49f-3676-42ee-b86c-72f338818097.zip |
| 63323-486 | GENERAL SURGERY KIT () KIT [CENTURION MEDICAL PRODUCTS] | 1 | Current NDC, Legacy NDC | 20140327_168ff921-70aa-45fd-80a7-6447a6d5dfe8.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63323-486-01 | ML - Milliliter | 63323-486 | 53575e7c-ec30-491c-800d-e2f2e0aab918 | 1 | 2019-12-10 |
| 63323-486-02 | ML - Milliliter | 63323-486 | 8c00d362-7eff-4deb-bf43-53a9506aa19d | 1 | 2019-12-10 |
| 63323-486-05 | ML - Milliliter | 63323-486 | 049b2b3b-0d23-4b00-92d8-5e2643ad5117 | 1 | 2019-12-10 |
| 63323-486-17 | ML - Milliliter | 63323-486 | 06027263-d174-40ea-9f34-cde0ccedc0f0 | 1 | 2012-07-24 |
| 63323-486-26 | ML - Milliliter | 63323-486 | 348a52bc-c28e-4315-a03e-952005b530ba | 1 | 2016-09-02 |
| 63323-486-27 | ML - Milliliter | 63323-486 | a4f02f5d-1dcd-46e2-beca-2e3e86b55cf3 | 1 | 2012-07-24 |
| 63323-486-41 | ML - Milliliter | 63323-486 | cd3d5dcc-bbe6-424b-ae62-a3b6f1ecaa11 | 1 | 2025-11-13 |
| 63323-486-57 | ML - Milliliter | 63323-486 | b3d735e0-3978-4c1e-b496-40a57da89c1e | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | A-S Medication Solutions | 82b377ee-0e3e-4cb9-a644-f45434c21cca | 2025-11-26 | Warnings, Adverse reactions | 1010033 V13007Z41A |
| Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Gel | THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GEL | Clarion Brands LLC | 445db02a-c8e8-6ebb-e063-6294a90a4301 | 2025-11-24 | Warnings | V13007Z41A |
| Natural Eyes Floaters Relief | CHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEA | TRP Company | 445dc831-195e-4b25-e063-6294a90a6efd | 2025-11-24 | Warnings | 451W47IQ8X |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | ProPharma Distribution | 42df73b0-20ee-d1aa-e063-6294a90aa275 | 2025-11-21 | Warnings, Adverse reactions | 1737761 V13007Z41A |
| Vital Female Sexual Energy | AGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, ONOSMODIUM VIRGINIANUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS | Liddell Laboratories, Inc. | 1ca43c82-62b0-4191-81a4-27f7f94109dd | 2025-11-20 | Warnings | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | Walgreen Company | d112a344-33cc-41d3-bae6-492631ebdba7 | 2025-11-19 | Warnings | 451W47IQ8X |
| Sodium chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | ce0c8c6f-734a-400f-9b60-a3b1e263f25f | 2025-11-18 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE TABLETS | Kesin Pharma Corporation | 2f107592-10c5-ef3b-e063-6394a90a7c0a | 2025-11-17 | Warnings | 451W47IQ8X |
| JUST CBD RELIEF SOOTHING | LIDOCAINE HCL | Just Brands LLC | f9aff6e7-5702-f61c-e053-6294a90aa66f | 2025-11-17 | Warnings | V13007Z41A |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Henry Schein, Inc. | 313a7e1f-c1a9-4fa5-bb83-7256c271b351 | 2025-11-17 | Warnings, Adverse reactions | V13007Z41A |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Henry Schein, Inc. | 335dfa50-56f3-4c02-b713-8eef4e28eb45 | 2025-11-17 | Warnings, Adverse reactions | V13007Z41A |
| Earthmed Soothe Chewable Orange | CITRIC ACID | Earthmed LLC | 439543fe-ceb9-4c5c-e063-6294a90a9b70 | 2025-11-14 | Warnings | 2968PHW8QP |
| ALUMIZEN | GARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, COPPER, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, LEAD, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED. | Natural Creations, Inc. | 4760ab09-1141-4944-b840-804ae6d86d2d | 2025-11-13 | Warnings | 451W47IQ8X |
| BLISTER HP | JUGLANS CINEREA BRANCH BARK/ROOT BARK, POTASSIUM IODIDE, LYCOPODIUM CLAVATUM SPORE, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, RANUNCULUS BULBOSUS, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG. | Natural Creations, Inc. | e76f05e7-6d7b-4d2e-ba26-bf776bf0e657 | 2025-11-13 | Warnings | 451W47IQ8X |
| Anxiety HP | ARSENIC TRIOXIDE, CALCIUM CARBONATE, STRYCHNOS IGNATII SEED, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA | Natural Creations, Inc. | 13d92246-c20e-47a8-b88f-22da876fc545 | 2025-11-13 | Warnings | 451W47IQ8X |
| ANXIETY II HP | ACONITUM NAPELLUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACTIVATED CHARCOAL, HUMAN BREAST TUMOR CELL, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF | Natural Creations, Inc. | 02fa45a5-08e1-41ad-acd4-0f85db07e89e | 2025-11-13 | Warnings | 451W47IQ8X |
| Launch Medical | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | 293ef514-44c1-43ac-9a81-c30e34ad39e5 | 2025-11-12 | Warnings | V13007Z41A |
| Tattoo Numbing Cream Co | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | 2a64b3ef-ed2d-49db-996d-f63ffecb5a1e | 2025-11-12 | Warnings | V13007Z41A |
| Painless Tattoo Numbing | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | efd3289f-dfb2-487c-a76f-00fe8af414e3 | 2025-11-12 | Warnings | V13007Z41A |
| Now Numb Numbing Cream | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | fed833f5-4f76-46e8-8ae1-655a9e576f70 | 2025-11-12 | Warnings | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.