Benzocaine 20%
- Product NDC
- 0121-1077
- 11-digit product format
- 001211077
- Labeler code
- 0121
- Product ID
- 0121-1077_83139f6d-1d4d-47d5-8da5-5dad5b9fe3b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine 20%
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-20
- Substance
- BENZOCAINE
- Active strength
- 200 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
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
- Benzocaine 20%
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOCAINE | 200 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| U3RSY48JW5 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 308657 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7fbce9a5-00dc-4a4a-8709-ab752bdf2f59 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0121-1077-01 | Benzocaine 20% | 1 in 1 POUCH | SOLUTION | 1 | 4 | |
| 0121-1077-01 | Benzocaine 20% | 0.5 mL in 1 APPLICATOR | SOLUTION | 0.5 | 4 | |
| 0121-1077-25 | Benzocaine 20% | 25 in 1 CARTON | SOLUTION | 25 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0121-1077-01 | EA - Each | 0121-1077 | 463d4083-6886-4ef3-81c8-72e6ce3353c8 | 1 | 2026-04-20 |
| 0121-1077-25 | EA - Each | 0121-1077 | 4bc3ba88-92f7-4ef2-9b52-2bd6f5179c10 | 1 | 2026-04-20 |
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 |
|---|---|---|---|---|---|---|
| CHLORASEPTIC | MENTHOL AND BENZOCAINE | Prestige Brands Holdings, Inc. | b30e4b32-89dd-4e53-81d5-1415105361d4 | 2024-10-25 | Warnings | M022 |
| Finafta MultiOral | BENZOCAINE | Efficient Laboratories Inc. | 28c5a993-fb5f-4091-af15-32ccae4b9a7d | 2024-10-14 | Warnings | M022 |
| Rexall Sensitive Freshmint | POTASSIUM NITRATE, SODIUM FLUORIDE | Old East Main CO. | 7e715bb9-666e-4de4-ba70-1c84f5243443 | 2024-10-14 | Warnings | M022 |
| Rexall Sensitive Extra Whitening | POTASSIUM NITRATE, SODIUM FLUORIDE | Old East Main CO. | 2daf18a3-f71e-4585-8128-4663eff7eb6d | 2024-10-14 | Warnings | M022 |
| Anadent Kanka Gel | BENZOCAINE | BELMORA LLC | e0f73d78-5db1-43b4-8f58-e5410ca4560f | 2024-10-04 | Warnings | M022 |
| Listerine Cool Mint Antiseptic | EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL | Navajo Manufacturing Company Inc. | f5f26e2f-8a1f-4687-e053-2a95a90ae378 | 2024-10-03 | Warnings | M022 |
| Colgate Great Regular Flavor | SODIUM MONOFLUOROPHOSPHATE | Navajo Manufacturing Company Inc. | f89bf259-b738-8229-e053-6394a90a0c59 | 2024-10-03 | Warnings | M022 |
| Colgate Total SF Clean Mint | STANNOUS FLUORIDE | Navajo Manufacturing Company Inc. | f71c53e0-e2dd-16f9-e053-6394a90accff | 2024-10-03 | Warnings | M022 |
| Crest Pro Health | CETYLPYRIDINIUM CHLORIDE | Navajo Manufacturing Company Inc. | 65bf17a9-21ad-27cb-e053-2991aa0afc40 | 2024-10-02 | Warnings | M022 |
| Sensodyne Pronamel Gentle Whitening Advanced | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 94e07979-943b-45bb-8e2b-90d686f3692e | 2024-09-04 | Warnings | M022 |
| Sensodyne Pronamel Gentle Whitening Advanced Plus | POTASSIUM NITRATE, SODIUM FLUORIDE | Haleon US Holdings LLC | 6eb304dd-2a24-4fa0-9d39-71264e88dd16 | 2024-08-29 | Warnings | M022 |
| Sensodyne Pronamel Clinical Enamel Strength Deep Clean | POTASSIUM NITRATE, SODIUM FLUORIDE | Haleon US Holdings LLC | cfda7efa-86fa-470d-a79f-81907e31778a | 2024-08-14 | Warnings | M022 |
| Sensodyne Pronamel Kids Bubble Twist | SODIUM FLUORIDE | Haleon US Holdings LLC | e403529a-0fac-4dab-b75c-46906add096b | 2024-08-13 | Warnings | M022 |
| Calcium Carbonate Assorted Flavors | ANTACID TABLETS | NuCare Pharmaceuticals,Inc. | af10dfb6-fef3-3410-e053-2995a90a9130 | 2024-07-17 | Warnings | M022 |
| SENSODYNE Advanced Whitening Plus | POTASSIUM NITRATE | Haleon US Holdings LLC | f757ccdd-b316-4799-a34a-10edbb73da6b | 2024-07-12 | Warnings | M022 |
| dentalux SENSITIVE ANTI-CAVITY FLUORIDE | POTASSIUM NITRATE, SODIUM FLUORIDE | Lidl US, LLC | baef7f15-8082-4e61-8c08-8beda8ad40c0 | 2024-07-03 | Warnings | M022 |
| Acetaminophen | ACETAMINOPHEN | NuCare Pharmaceuticals,Inc. | 872365ca-0c6b-550a-e053-2a91aa0ab25a | 2024-06-14 | Warnings | M022 |
| Amosan Oral Wound Cleanser Spearmint | SODIUM PERBORATE MONOHYDRATE | Vintage Brands Limited | 7ac6c649-758f-4128-9920-466c0967b86a | 2024-05-21 | Warnings | M022 |
| Sensodyne | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 9e8e7b9f-3ccd-4935-b886-93f3a5045b67 | 2024-05-15 | Warnings | M022 |
| Sensodyne Extra Whitening | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 1ed4a62b-f1d3-4740-8150-b94e02398740 | 2024-05-15 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | PSN | 7fbce9a5-00dc-4a4a-8709-ab752bdf2f59 | 4 |
| 308657 | benzocaine 200 MG/ML Mucous Membrane Topical Solution | SCD | 7fbce9a5-00dc-4a4a-8709-ab752bdf2f59 | 4 |
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | SY | 7fbce9a5-00dc-4a4a-8709-ab752bdf2f59 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0121-1077-01 | 00121107701 | 1 in 1 POUCH | Historical | ||||
| 0121-1077-25 | 00121107725 | 25 POUCH in 1 CARTON (0121-1077-25) / 1 APPLICATOR in 1 POUCH (0121-1077-01) / .5 mL in 1 APPLICATOR | 25 pouch | 2026-03-20 | No | No | Current |