Orajel Cold Sore Touch Free - Single Dose
- Product NDC
- 10237-798
- 11-digit product format
- 102370798
- Labeler code
- 10237
- Product ID
- 10237-798_51b6fb8e-eeba-a04a-e063-6294a90a610f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride, Benzocaine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-09-01
- Substance
- BENZALKONIUM CHLORIDE; BENZOCAINE
- Active strength
- 1.3; 50 mg/mL; mg/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded product | product | ad56d346431e… | cc804d4bbf1e… | |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 10237-798-35 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded product | product | 367a005e9d99… | 383a685ebd0f… | |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 10237-798-35 | 367a005e9d99… | 383a685ebd0f… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Orajel Cold Sore Touch Free - Single Dose
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
| BENZOCAINE | 50 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5UM2KM3W7 | Internal UNII lookup |
| U3RSY48JW5 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2572114 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ce40829e-941f-2548-e053-2995a90a1e0e | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2024-11-27 | Orajel Cold Sore Touch Free - Single Dose |
| 2024-11-27 | Orajel Cold Sore Touch Free - Single Dose |
| 2024-07-30 | Orajel Cold Sore Touch Free - Single Dose |
| 2024-07-30 | Orajel Cold Sore Touch Free - Single Dose |
| 2024-02-06 | Orajel Cold Sore Touch Free - Single Dose |
| 2024-02-06 | Orajel Cold Sore Touch Free - Single Dose |
| 2023-01-30 | Orajel Cold Sore Touch Free - Single Dose |
| 2023-01-30 | Orajel Cold Sore Touch Free - Single Dose |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10237-798-35 | Orajel Cold Sore Touch Free - Single Dose | 3.5 mL in 1 VIAL, SINGLE-DOSE | LIQUID | 3.5 | 6 | |
| 10237-798-35 | Orajel Cold Sore Touch Free - Single Dose | 6 in 1 PACKAGE | LIQUID | 6 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10237-798 | ORAJEL COLD SORE TOUCH FREE - SINGLE DOSE (BENZALKONIUM CHLORIDE, BENZOCAINE) LIQUID [CHURCH & DWIGHT CO., INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250330_ce40829e-941f-2548-e053-2995a90a1e0e.zip |
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 |
|---|---|---|---|---|---|---|
| AleveX | CAMPHOR AND MENTHOL | Bayer HealthCare LLC | bc66bc1b-c0d5-2481-e053-2a95a90a75de | 2025-12-04 | Warnings | M017 |
| AleveX | CAMPHOR AND MENTHOL | Bayer HealthCare LLC | bafd199a-e198-d5d1-e053-2995a90ad1cb | 2025-12-04 | Warnings | M017 |
| AleveX | CAMPHOR AND MENTHOL | Bayer HealthCare LLC | bafdf06b-25f5-e29e-e053-2a95a90a5e1b | 2025-12-04 | Warnings | M017 |
| Milagroso | METHYL SALICYLATE | Pharmadel LLC | fdcc8f44-afa0-3af0-e053-6394a90aa46d | 2025-12-04 | Warnings | M017 |
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35221a-2fcb-2735-e063-6294a90a88ca | 2025-12-04 | Warnings | M017 |
| Pain Relieving | TROLAMINE SALICYLATE | CARDINAL HEALTH 110, LLC. DBA LEADER | b813262e-57c6-4d2c-8cc0-7a17f6f59343 | 2025-12-04 | Warnings | M017 |
| Gold Bond Medicated Extra Strength Body | MENTHOL | Gold Bond Co LLC | 7b75b7de-9c0b-4edf-b923-320f7d2bb1e6 | 2025-12-04 | Warnings | M017 |
| Lidocaine Patch | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 38767081-7011-6602-e063-6394a90a2784 | 2025-12-03 | Warnings | M017 |
| 4% Lidocaine Maximum Strength Pain Relief | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 3e5a5165-a773-0501-e063-6294a90ae2f4 | 2025-12-03 | Warnings | M017 |
| Leader Lidocaine | LIDOCAINE HCL | CARDINAL HEALTH | cece6765-0e2f-5ce9-e053-2995a90a3758 | 2025-12-03 | Warnings | M017 |
| Westlake Lidocaine | LIDOCAINE HCL | Westlake Pharma LLC | 0c586a14-1a2a-9f42-e063-6294a90a16c1 | 2025-12-03 | Warnings | M017 |
| CVS Lidocaine Maximum Strength | LIDOCAINE HCL | CVS Pharmacy | 87490c0f-a4d9-740e-e053-2a95a90a4724 | 2025-12-03 | Warnings | M017 |
| CVS Maximum Strength Burn | LIDOCAINE HYDROCHLORIDE 4% | CVS Pharmacy | 4510f379-c5a4-92c3-e063-6294a90a0a32 | 2025-12-03 | Warnings | M017 |
| LidoPatch Pain Relief | LIDOCAINE, MENTHOL | JAR Laboratories | 07289aa1-43ed-df31-e063-6394a90a764a | 2025-12-03 | Warnings | M017 |
| Equate Pain Relief Cream | 4% LIDOCAINE HCL | Walmart, Inc | 7d8e8a9a-5474-4c7b-e053-2991aa0a29f5 | 2025-12-03 | Warnings | M017 |
| Solarcaine Burn Pain Relief 4oz | SOLARCAINE BURN PAIN RELIEF 4OZ | WellSpring Pharmaceutical Corporation | 14f23c28-c713-4868-9f46-66363bf94b2c | 2025-12-03 | Warnings | M017 |
| ElixirCortiRelief | HYDROCORTISONE | ELIXIR HEALTHCARE USA, LLC. | a6ca66f3-9759-4c98-a758-45700bc08352 | 2025-12-02 | Warnings | M017 |
| Pain Relief Gel-Patch | LIDOCAINE 4% | Trifecta Pharmaceuticals USA, LLC. | 12a27ce7-c547-7134-e063-6394a90a94bd | 2025-12-02 | Warnings | M017 |
| 5Kind DMSO | MENTHOL, METHYL SALICYLATE | 5KIND TRADING LTD | 6a6c7241-f544-4784-9581-f5b172fdbec7 | 2025-12-02 | Warnings | M017 |
| PEDIADERMICS ECZEMA 2 | HYDROCORTISONE | RENU LABORATORIES, LLC | da840bf6-ed65-bafc-e053-2a95a90a92d5 | 2025-12-02 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2572114 | benzalkonium chloride 0.13 % / benzocaine 5 % Topical Solution | PSN | ce40829e-941f-2548-e053-2995a90a1e0e | 6 |
| 2572114 | benzalkonium chloride 1.3 MG/ML / benzocaine 50 MG/ML Topical Solution | SCD | ce40829e-941f-2548-e053-2995a90a1e0e | 6 |
| 2572114 | benzalkonium chloride 0.13 % / benzocaine 5 % Topical Solution | SY | ce40829e-941f-2548-e053-2995a90a1e0e | 6 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 10237-798-35 | 10237079835 | 6 VIAL, SINGLE-DOSE in 1 PACKAGE (10237-798-35) / 3.5 mL in 1 VIAL, SINGLE-DOSE | 2021-09-01 | 0000-00-00 | No | No | Current |