NDC 10742-8902-01 - Red Cross Oral Pain Relief
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
- 10742-8902
- Requested NDC
- 10742-8902-01
- Package NDCs from labels
- 10742-8902-1, 10742-8902-01
- Manufacturer
- The Mentholatum Company
- Effective date
- 2024-12-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Red Cross Oral Pain Relief - The Mentholatum Company | The Mentholatum Company | 2024-12-17 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10742-8902-1 | 2023-02-07 | C162847 | 48780-1 | f386c64a-36a2-0266-e053-dadaa90a7c1a | Drug Facts - Red Cross Oral Pain Relief |
| 10742-8902-1 | 2023-01-30 | C162847 | 48780-1 | f386c64a-36a2-0266-e053-dadaa90a7c1a | Drug Facts - Red Cross Oral Pain Relief |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10742-8902-1 | Red Cross Oral Pain Relief | 3.7 mL in 1 BOTTLE | LIQUID | 3.7 | 5 | |
| 10742-8902-1 | Red Cross Oral Pain Relief | 1 in 1 BLISTER PACK | LIQUID | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10742-8902 | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241219_cbd41429-f730-4577-9f06-ef1831cf62e1.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZOCAINE | ACTIVE INGREDIENT | U3RSY48JW5 | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 2 | |
| BENZOCAINE | ACTIVE MOIETY | U3RSY48JW5 | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 2 | |
| AMMONIUM GLYCYRRHIZATE | INACTIVE INGREDIENT | 3VRD35U26C | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 2 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 2 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 2 | |
| SACCHARIN CALCIUM | INACTIVE INGREDIENT | 5101OP7P2I | RED CROSS ORAL PAIN RELIEF (BENZOCAINE) LIQUID [THE MENTHOLATUM COMPANY] | 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 |
|---|---|---|---|---|---|---|
| BiteMD | INSECT BITE RELIEF | Wisconsin Pharmacal Company | 4f860c1e-a638-4923-e063-6294a90ae7e2 | 2026-04-15 | Warnings | U3RSY48JW5 |
| Osstem S Sensitivity relief tooth | POTASSIUM NITRATE, SODIUM FLUORIDE | Osstem Pharma Co., Ltd | 4f8ab179-8f29-a7cf-e063-6294a90a0c22 | 2026-04-15 | Warnings | M022 |
| Crest Pro-Health Gum DetoxifyWinter Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6db58f-0b09-d155-e063-6394a90ae658 | 2026-04-14 | Warnings | M022 |
| Lolleez Orange Mango | PECTIN | BFY LLC | 4f6dec8b-078a-f321-e063-6294a90a248c | 2026-04-14 | Warnings | M022 |
| Crest Pro-Health Gum Restore Smooth Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6e3b36-e565-7d27-e063-6294a90ae5ac | 2026-04-14 | Warnings | M022 |
| Crest Pro-Health Nightly Bacteria Shield | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6ec1e0-c6b5-226f-e063-6294a90a8f14 | 2026-04-14 | Warnings | M022 |
| Sting Relief Swab | BENZOCAINE | 4 Visions LLC | 4f76a8c5-fde6-eee0-e063-6394a90a09f8 | 2026-04-14 | Warnings | U3RSY48JW5 |
| AHLO PRO Healthy Gums | CETYLPYRIDINIUM CHLORIDE | Gervest USA Inc | 4f5a0ccb-26e5-ebb6-e063-6394a90abbc5 | 2026-04-13 | Warnings | M022 |
| Artificial Tears Lubricant Eye Drops | GLYCERIN, PROPYLENE GLYCOL | CVS Pharmacy | 28297fee-8185-4869-8f39-5bfbf8bf8bfd | 2026-04-13 | Warnings | 6DC9Q167V3 |
| Retaine Ultra PF | POLYETHYLENE GLYCOL | OCuSOFT LLC | a5aaaf06-772d-44d3-8601-f978ddc48ad7 | 2026-04-13 | Warnings | 6DC9Q167V3 B697894SGQ |
| Crest Scope Original Clean Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f1db6f4-acd7-a665-e063-6294a90a826b | 2026-04-10 | Warnings | M022 |
| Sore Throat | PHENOL GLYCERIN | Walgreens | 1e845299-178e-49ce-9d08-7e9d548a5a6d | 2026-04-09 | Warnings | M022 |
| Sore throat cherry | PHENOL | Walgreens | 67bed85e-e1e2-49ba-98d6-dfd4e1cd6856 | 2026-04-08 | Warnings | M022 |
| Health-Tec Topical Anesthetic | BENZOCAINE | Dental Health Products, Inc. | 5eb437c5-a2af-4c0d-b7b9-9ab7d093db85 | 2026-04-06 | Warnings | M022 U3RSY48JW5 |
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Family Dollar (FAMILY WELLNESS) | 269b9e7f-c5c8-4023-a3ea-e39040ade271 | 2026-04-06 | Warnings | M022 |
| Health-Tec Topical Anesthetic | BENZOCAINE | Dental Health Products, Inc. | c3fb6705-c647-4fe6-9aca-29735d01d8ea | 2026-04-02 | Warnings | M022 U3RSY48JW5 |
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Family Dollar (FAMILY WELLNESS) | f061ec82-7f0e-4b93-afa6-ae9fe14ab4ea | 2026-04-01 | Warnings | M022 |
| CloSYS Silver Healthy Gums | CETYLPYRIDINIUM CHLORIDE | Rowpar Pharmaceuticals, Inc. | 11fd3f31-ee0c-43d2-a856-929d1298277c | 2026-04-01 | Warnings | M022 |
| Crest Pro-Health Bold Fresh Breath | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 5692c0ce-a914-08c4-e063-6394a90adf15 | 2026-04-01 | Warnings | M022 |
| Anticavity Fluoride | SODIUM FLUORIDE AND ACIDULATED PHOSPHATE | Family Dollar (FAMILY WELLNESS) | 1666fff6-9a8b-40f9-ae53-914152db386b | 2026-04-01 | Warnings | M022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.