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 |
|---|---|---|---|---|---|---|
| Stress Away Anxiety Relief | ACONITUM NAP, ALFALFA, AVENA, CHAMOMILLA, GELSEMIUM, HUMULUS IUPULUS, IGNATIA, KALI ARS, KALI PHOS, MURIATICUM AC, NAT PHOS, PASSIFLORA, PHOSPHORUS, STAPHYSAGRIA, STRAMONIUM | Silver Star Brands | 05e04129-e7c1-4e11-e063-6394a90a09ca | 2025-01-01 | Warnings | QTT17582CB |
| OKeeffes Working Hands Pain Relief Skin Protectant | ALLANTOIN, LIDOCAINE HYDROCHLORIDE | The Gorilla Glue Company/O'Keeffe's Company | 0685da25-c9fa-e1cd-e063-6394a90ae1b3 | 2025-01-01 | Warnings | V13007Z41A |
| Pain Relieving Cream Lidocaine | BENZYL ALCOHOL, LIDOCAINE HCI | Trifecta Pharmaceuticals USA LLC | 039a2036-54b2-cf28-e063-6294a90a8ce6 | 2024-12-31 | Warnings | V13007Z41A |
| Lidocaine hydrochloride | LIDOCAINE HYDROCHLORIDE | Advanced Rx Pharmacy of Tennessee, LLC | f4c19cf5-c8b1-5e9f-e053-2995a90aee53 | 2024-12-31 | Warnings, Adverse reactions | V13007Z41A |
| KEEPAN A | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | Sato Pharmaceutical Co., Ltd. | a30679d5-5507-499d-9d9f-498095fd32ac | 2024-12-30 | Warnings | V13007Z41A |
| Rain Renewal Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Rain Eye Drops, LLC | af7a5768-7d1d-3d93-e053-2a95a90a38f6 | 2024-12-29 | Warnings | K679OBS311 |
| pain relief roll-on | LIDOCAINE 4% | Bionpharma Inc. | f607b6dc-8d13-604a-e053-2995a90a59ab | 2024-12-23 | Warnings | V13007Z41A |
| Household Antigens | ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUM | Energique, Inc. | f3db63df-62a4-48d6-92e7-94e4a5701552 | 2024-12-20 | Warnings | Z8IX2SC1OH A2I8C7HI9T |
| Pain Itch Relief | LIDOCAINE HCI | Trifecta Pharmaceutical USA LLC | f40b19a8-795c-f514-e053-2a95a90a6d15 | 2024-12-20 | Warnings | V13007Z41A |
| DCH Burn Relief | LIDOCAINE HCL | Derma Care Research Labs, LLC | ff227154-cf3b-9796-e053-6294a90a5535 | 2024-12-20 | Warnings | V13007Z41A |
| Meijer Pain Relief | LIDOCAINE HCL 4% | Meijer | f31b11ed-2ff9-5cfc-e053-2a95a90af2ca | 2024-12-20 | Warnings | V13007Z41A |
| Leader | LIDOCAINE HCL | Cardinal Health | cea6bd2d-a265-1209-e053-2995a90ab0a5 | 2024-12-19 | Warnings | V13007Z41A |
| DCH Nerve Pain Relief Roll-On | LIDOCAINE HCL 4%, MENTHOL 1% | Derma Care Research Labs, LLC | ff32cbb2-79eb-9158-e053-6394a90ac357 | 2024-12-19 | Warnings | V13007Z41A |
| DCH Pain Relief Roll-On | LIDOCAINE HCL 4% | Derma Care Research Labs, LLC | fda35d37-f36e-efc8-e053-6294a90a2bb8 | 2024-12-19 | Warnings | V13007Z41A |
| Warrior Pain Relief Roll-On Maximum Strength | LIDOCAINE HCL 4% | Derma Care Research Labs, LLC | dd80e560-6467-2166-e053-2995a90a88a8 | 2024-12-19 | Warnings | V13007Z41A |
| Warrior Burn Relief Aloe Maximum Strength | LIDOCAINE HCL 4% | Derma Care Research Labs, LLC | ec6efa4b-dcbe-1c2b-e053-2995a90ae043 | 2024-12-19 | Warnings | V13007Z41A |
| DCH Pain Relief | LIDOCAINE HCL 4% | Derma Care Research Labs, LLC | 00dd70f3-ecc3-33ba-e063-6294a90a4f32 | 2024-12-19 | Warnings | V13007Z41A |
| HealthWise 4% Lidocaine Cream | LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | 0fb2af30-7f2d-c7c4-e063-6294a90a37f7 | 2024-12-19 | Warnings | V13007Z41A |
| CVS Health Lidocaine Pain Relief | LIDOCAINE HCL | CVS Pharmacy | 445b0778-7266-4e72-97cc-e9e0d0066b61 | 2024-12-18 | Warnings | V13007Z41A |
| First Aid Only First Aid-Burn | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | Acme United Corporation | f31a44ff-e4ac-de1e-e053-2a95a90ab036 | 2024-12-18 | Warnings | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.