Oral Pain Relief
- Product NDC
- 52000-060
- 11-digit product format
- 520000060
- Labeler code
- 52000
- Product ID
- 52000-060_de98c97f-7c6f-4676-bf8e-797f3f24c598
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine and Benzalkonium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-05
- Substance
- BENZOCAINE; BENZALKONIUM CHLORIDE
- Active strength
- .2; .01 g/g; g/g
- 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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 52000-060 | I | Inactivated by FDA | 2026-10-21 | ||
| excluded package | package | 52000-060 | 52000-060-01 | I | Inactivated by FDA | 2026-10-21 |
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 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 52000-060-01 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 52000-060-01 | f5e01cc5f278… | a2eaf40c39c3… |
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
- Oral Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOCAINE | .2 g/g |
| BENZALKONIUM CHLORIDE | .01 g/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| U3RSY48JW5 | Internal UNII lookup |
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1595155 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 18520f9b-4d35-1e9c-e063-6294a90aaa39 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52000-060-01 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-2e7e-fb37-e063-e6dba90a4e07 | Oral Pain Relief Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52000-060-01 | Oral Pain Relief | 14 g in 1 TUBE | GEL | 14 | 4 | |
| 52000-060-01 | Oral Pain Relief | 1 in 1 CARTON | GEL | 1 | 4 | |
| 52000-060-02 | Oral Pain Relief | 14 g in 1 TUBE | GEL | 14 | 3 | |
| 52000-060-02 | Oral Pain Relief | 1 in 1 CARTON | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52000-060 | ORAL PAIN RELIEF (BENZOCAINE AND BENZALKONIUM CHLORIDE) GEL [UNIVERSAL DISTRIBUTION CENTER LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241212_baf0cf27-052e-4367-9a6e-75038b97a051.zip |
| 52000-060 | ORAL PAIN RELIEF (BENZOCAINE AND BENZALKONIUM CHLORIDE) GEL [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241218_18520f9b-4d35-1e9c-e063-6294a90aaa39.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 |
|---|---|---|---|---|---|---|
| Patterson Dental Topical Anesthetic | BENZOCAINE | Patterson Dental | 3f19a1a7-c234-8d26-e063-6394a90ad7e9 | 2025-09-18 | Warnings | M022 |
| McKesson Orasol Gel | BENZOCAINE 20% | McKesson Medical-Surgical | cc8724f4-c482-5e7d-e053-2a95a90a608f | 2025-09-09 | Warnings | M022 |
| MGC Health Drops Sugar Free Lemon Mint | MENTHOL | Medical Group Care LLC | 3d70bca7-e830-e693-e063-6294a90a73f9 | 2025-08-28 | Warnings | M022 |
| Exchange Select Drops Sugar Free Lemon Mint | MENTHOL | Army & Air Force Exchange Service | 3d70450f-04ea-1885-e063-6294a90a05bd | 2025-08-28 | Warnings | M022 |
| Ki No Sin | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 21fa2bad-5b8b-8aac-e063-6394a90a9f49 | 2025-08-27 | Warnings | M022 |
| R Cos | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 21fa767a-1344-5ed9-e063-6394a90a5fe6 | 2025-08-27 | Warnings | M022 |
| Na Mi Cal | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 20cfbcd1-eb13-933c-e063-6294a90a7e59 | 2025-08-27 | Warnings | M022 |
| Ki No Sin | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 20cf8f80-c638-4d94-e063-6294a90a5400 | 2025-08-27 | Warnings | M022 |
| Charm Tex FLUORIDE | SODIUM MONOFLUOROPHOSPHATE | Yangzhou Hongshengding Chemical Co.,Ltd. | 63a69664-8611-4d69-b871-8d1d5b553e5c | 2025-08-18 | Warnings | M022 |
| QUALITY CHOICE SALINE | SODIUM CHLORIDE | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) | f51491d8-12ad-4b1b-a171-c621bfdcc341 | 2025-08-12 | Warnings | M022 |
| MGC Health Drops Sugar Free Lemon Mint | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | b9227966-847c-40c3-87f2-8bea3954ec84 | 2025-08-12 | Warnings | M022 |
| Exchange Select Drops Sugar Free Lemon Mint | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 5f4b1960-43ac-4c74-9410-210c48bd8a1b | 2025-08-12 | Warnings | M022 |
| HurriCaine Topical Anesthetic | BENZOCAINE | Beutlich Pharmaceuticals, LLC | 113cdb83-0fdd-40f2-8ee6-b771dca99713 | 2025-08-12 | Warnings | M022 |
| CVS Pharmacy Maximum Strength | BENZOCAINE | CVS Pharmacy | 13bf31c1-78e3-459f-9249-b0b6e2c17a13 | 2025-08-12 | Warnings | M022 |
| Rexall Maximum Strength | BENZOCAINE | Rexall | 8f6e2780-cfb7-4bef-9b7d-13cb80d8923e | 2025-08-12 | Warnings | M022 |
| Walgreens Maximum Strength | BENZOCAINE | Walgreens | 8f24309d-d393-455a-a9a5-a55344adf36b | 2025-08-12 | Warnings | M022 |
| Oral Anesthetic Liquid | BENZOCAINE | Meijer, Inc. | 0321c480-e150-421d-e063-6294a90ad687 | 2025-08-12 | Warnings | M022 |
| Walgreens Mouth Sore Relief | BENZOCAINE | Walgreens | 253d7ea2-e48e-c7d7-e063-6394a90ae001 | 2025-08-12 | Warnings | M022 |
| Charm Tex FLUORIDE Gel | SODIUM FLUORIDE | Yangzhou Hongshengding Chemical Co.,Ltd. | 897b0102-1c96-4699-908e-a7b7e26cd29f | 2025-08-08 | Warnings | M022 |
| Meijer Enamel Guard | POTASSIUM NITRATE, SODIUM FLUORIDE | Meijer Distribution Inc | 82bc95be-0a07-3f00-e053-2a91aa0a7438 | 2025-08-08 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1595155 | benzocaine 20 % / benzalkonium chloride 0.1 % Oral Gel | PSN | baf0cf27-052e-4367-9a6e-75038b97a051 | 4 |
| 1595155 | benzalkonium chloride 0.001 MG/MG / benzocaine 0.2 MG/MG Oral Gel | SCD | baf0cf27-052e-4367-9a6e-75038b97a051 | 4 |
| 1595155 | benzalkonium chloride 0.1 % / benzocaine 20 % Oral Gel | SY | baf0cf27-052e-4367-9a6e-75038b97a051 | 4 |
| 1595155 | benzocaine 20 % / benzalkonium chloride 0.1 % Oral Gel | PSN | 18520f9b-4d35-1e9c-e063-6294a90aaa39 | 3 |
| 1595155 | benzalkonium chloride 0.001 MG/MG / benzocaine 0.2 MG/MG Oral Gel | SCD | 18520f9b-4d35-1e9c-e063-6294a90aaa39 | 3 |
| 1595155 | benzalkonium chloride 0.1 % / benzocaine 20 % Oral Gel | SY | 18520f9b-4d35-1e9c-e063-6294a90aaa39 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 52000-060-01 | 52000006001 | 1 TUBE in 1 CARTON (52000-060-01) > 14 g in 1 TUBE | 1 tube | 2020-12-09 | 0000-00-00 | No | No | Current |
| 52000-060-02 | 52000006002 | 1 TUBE in 1 CARTON (52000-060-02) / 14 g in 1 TUBE | 1 tube | 2024-05-01 | No | No | Current |