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 | Type |
|---|---|---|---|
| Lidocaine Hydrochloride Oral Topical Solution USP, 2% (Viscous) | ATLANTIC BIOLOGICALS CORP. | 2025-05-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-0138-1 | Lidocaine hydrochloride | 50 in 1 BOX, UNIT-DOSE | SOLUTION | 50 | 3 | |
| 17856-0138-2 | Lidocaine hydrochloride | 50 in 1 BOX, UNIT-DOSE | SOLUTION | 50 | 3 | |
| 17856-0138-3 | Lidocaine hydrochloride | 15 mL in 1 CUP, UNIT-DOSE | SOLUTION | 15 | 3 | |
| 17856-0138-4 | Lidocaine hydrochloride | 20 mL in 1 CUP, UNIT-DOSE | SOLUTION | 20 | 3 | |
| 17856-0138-5 | Lidocaine hydrochloride | 72 in 1 BOX, UNIT-DOSE | SOLUTION | 72 | 3 | |
| 17856-0138-6 | Lidocaine hydrochloride | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-0138 | LIDOCAINE HYDROCHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 3 | Current NDC, 6 package rows | 20250514_75d17334-6876-42d0-8a02-82669d139e4f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17856-0138-1 | ML - Milliliter | 17856-0138 | c494c261-df59-4696-919e-e062bcc63ab6 | 1 | 2024-03-12 |
| 17856-0138-2 | ML - Milliliter | 17856-0138 | c72c7dce-4880-4309-b60c-c5d0f465dce5 | 1 | 2024-03-12 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| 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 |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | ProPharma Distribution | 42df73b0-20ee-d1aa-e063-6294a90aa275 | 2025-11-21 | Warnings, Adverse reactions | V13007Z41A |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| Walgreens Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Walgreen Company | a39864a3-2407-7b7e-e053-2a95a90ab92f | 2025-11-19 | Warnings | K679OBS311 |
| Walgreens Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Walgreen Company | a39919d5-84db-05df-e053-2995a90ab1d2 | 2025-11-19 | Warnings | K679OBS311 |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| 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 |
| 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.