NDC 61010-5000-01 - 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
- 61010-5000
- Requested NDC
- 61010-5000-01
- Package NDCs from labels
- 61010-5000-0, 61010-5000-1, 61010-5000-3, 61010-5000-4, 61010-5000-5, 61010-5000-6, 61010-5000-01
- Manufacturer
- Safetec of America, Inc.
- Effective date
- 2024-02-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 61010-5000, Burn Gel | Safetec of America, Inc. | 2024-02-07 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 61010-5000-0 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-1 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-3 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-4 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-5 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-6 | 2024-02-07 | 61010-5000, Burn Gel |
| 61010-5000-0 | 2024-01-30 | 61010-5000, Burn Gel |
| 61010-5000-1 | 2024-01-30 | 61010-5000, Burn Gel |
| 61010-5000-3 | 2024-01-30 | 61010-5000, Burn Gel |
| 61010-5000-4 | 2024-01-30 | 61010-5000, Burn Gel |
| 61010-5000-5 | 2024-01-30 | 61010-5000, Burn Gel |
| 61010-5000-6 | 2024-01-30 | 61010-5000, Burn Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61010-5000-0 | Lidocaine Hydrochloride | 3.3 g in 1 PACKET | GEL | 3.3 | 5 | |
| 61010-5000-1 | Lidocaine Hydrochloride | 121.2 g in 1 BOTTLE | GEL | 121.2 | 5 | |
| 61010-5000-3 | Lidocaine Hydrochloride | 0.9 g in 1 POUCH | GEL | 0.9 | 5 | |
| 61010-5000-4 | Lidocaine Hydrochloride | 144 in 1 CARTON | GEL | 144 | 5 | |
| 61010-5000-4 | Lidocaine Hydrochloride | 0.9 g in 1 POUCH | GEL | 0.9 | 5 | |
| 61010-5000-5 | Lidocaine Hydrochloride | 0.9 g in 1 POUCH | GEL | 0.9 | 5 | |
| 61010-5000-5 | Lidocaine Hydrochloride | 25 in 1 CARTON | GEL | 25 | 5 | |
| 61010-5000-6 | Lidocaine Hydrochloride | 0.9 g in 1 PACKET | GEL | 0.9 | 5 | |
| 61010-5000-6 | Lidocaine Hydrochloride | 10 in 1 BOX | GEL | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61010-5000 | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 5 | Current NDC, Legacy NDC, 9 package rows | 20240208_1c5eb3b3-79b3-472a-ae36-ec6a7dc72925.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Lidocaine Hydrochloride | ACTIVE INGREDIENT | V13007Z41A | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| Lidocaine | ACTIVE MOIETY | 98PI200987 | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| .alpha.-tocopherol acetate | INACTIVE INGREDIENT | 9E8X80D2L0 | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| aloe vera leaf | INACTIVE INGREDIENT | ZY81Z83H0X | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| diazolidinyl urea | INACTIVE INGREDIENT | H5RIZ3MPW4 | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| menthol | INACTIVE INGREDIENT | L7T10EIP3A | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| propylene glycol | INACTIVE INGREDIENT | 6DC9Q167V3 | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| trolamine | INACTIVE INGREDIENT | 9O3K93S3TK | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | LIDOCAINE HYDROCHLORIDE GEL [SAFETEC OF AMERICA, INC.] | 2 |
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 |
|---|---|---|---|---|---|---|
| Rapid Relief | PAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 434df0be-49ff-aa56-e063-6394a90a3b5a | 2025-11-11 | Warnings | M017 L7T10EIP3A |
| TopCare Pain Relief Maximum Strength | LIDOCAINE HYDROCHLORIDE | TOPCO ASSOCIATES | b0ae3a7c-52d1-4923-bd50-6bb3749006c8 | 2025-11-11 | Warnings | M017 V13007Z41A |
| Comfortcaine | LIDOCAINE HCL | QS Key West Aloe, LLC | 831b7c11-e437-4e74-808e-c9c1eb8b82f6 | 2025-11-11 | Warnings | M017 V13007Z41A |
| A and E Marathon Delay Serum | DELAY SERUM | Phe Inc | 4355d1d8-44fe-aca1-e063-6294a90a85ff | 2025-11-11 | Warnings | M017 |
| A and E Deep Throat Desensitizing SprayStrawberry | ORAL NUMBING SPRAY STRAWBERRY | Phe Inc | 4355dab1-a293-ded6-e063-6394a90af9b0 | 2025-11-11 | Warnings | M017 |
| A and E Easy Anal Gel | ANAL NUMBING LUBRICANT | Phe Inc | 4355e0f3-65ba-eca6-e063-6394a90ab43c | 2025-11-11 | Warnings | M017 |
| A and E Deep Throat Desensitizing SprayPeppermint | ORAL NUMBING SPRAY MINT | Phe Inc | 4355e0d0-1222-d594-e063-6294a90abb29 | 2025-11-11 | Warnings | M017 |
| DermaNumb Analgesic | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 0ea46890-45c3-4732-bc47-227f7c67daf1 | 2025-11-11 | Warnings | M017 V13007Z41A |
| Derma Numb Pain Relief | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 710991ae-8f82-4893-93a7-0ef3f815d132 | 2025-11-11 | Warnings | M017 V13007Z41A |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Eugia US LLC | 5524cbfd-d6e6-42eb-aaa5-22495e0a86b6 | 2025-11-11 | Warnings, Adverse reactions | V13007Z41A |
| HYDROCORTISONE | HYDROCORTISONE | Encube Ethicals, Inc. | 969cd576-82d3-4662-bbc1-3587a1f6a564 | 2025-11-10 | Warnings | M017 |
| Jelcaine Sterile | LIDOCAINE HCL JELLY USP, 2% | Brookfield Pharmaceuticals, LLC | 1a39d1de-7aa2-3068-e063-6394a90aed85 | 2025-11-10 | Warnings | M017 1011852 V13007Z41A |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | c6e86a0f-6f9b-45b7-86ce-0bb1c198061a | 2025-11-10 | Warnings | M017 |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | 97ae1993-7268-4b7f-92e2-6004337d5650 | 2025-11-10 | Warnings | M017 |
| MENTHOL AND METHYL SALICYLATE | ELECTRIC MEDICATED BALM ULTRA STRENGTH | FEI FAH MEDICAL MANUFACTURING PTE LTD | 91e6d3b9-25bb-4015-9d96-bd27f93e5ada | 2025-11-10 | Warnings | M017 L7T10EIP3A |
| E MEI SHAN MEDICATED | CAMPHOR, MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | bda1e7c1-42df-4126-a512-80f843b07fd0 | 2025-11-10 | Warnings | M017 L7T10EIP3A |
| EXTRA STRENGTH HUA TUO PAIN RELIEVING | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | 9850754b-ac94-4ec6-b75a-8096e5ac9456 | 2025-11-10 | Warnings, Adverse reactions | M017 L7T10EIP3A |
| TONG FENG DING PAIN RELIEF | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | fe87b864-b3ee-4a4b-8e5a-e1ee6493de0d | 2025-11-10 | Warnings, Adverse reactions | M017 L7T10EIP3A |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 5ef90782-8201-47d1-b57f-f032d4c9b06a | 2025-11-10 | Warnings, Adverse reactions | M017 L7T10EIP3A |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 1388ab3a-c26f-427d-898d-0d88411a5fba | 2025-11-10 | Warnings, Adverse reactions | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.