HurriCaine
- Product NDC
- 0283-0569
- 11-digit product format
- 002830569
- Labeler code
- 0283
- Product ID
- 0283-0569_42f260d7-63f7-4356-e063-6394a90a4676
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- LIQUID
- Route
- DENTAL; ORAL; PERIODONTAL
- Labeler
- Beutlich Pharmaceuticals, LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1969-05-15
- Substance
- BENZOCAINE
- Active strength
- 200 mg/g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 package | package | 0283-0569 | 0283-0569-02 | D | Discontinued by firm | 2026-10-16 | |
| excluded package | package | 0283-0569 | 0283-0569-72 | D | Discontinued by firm | 2026-10-16 |
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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 0283-0569 | 0283-0569-72 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 0283-0569 | 0283-0569-02 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… |
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
- HurriCaine
- Brand name suffix
- Topical Anesthetic Liquid
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZOCAINE | 200 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| U3RSY48JW5 | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| fee9969d-ad1a-4f44-9741-a0a44c9e1128 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0283-0569-02 | HurriCaineTopical Anesthetic Liquid | 2 g in 1 APPLICATOR | LIQUID | 2 | 51 | |
| 0283-0569-17 | HurriCaineTopical Anesthetic Liquid | 1 g in 1 PACKET | LIQUID | 1 | 51 | |
| 0283-0569-31 | HurriCaineTopical Anesthetic Liquid | 29.6 g in 1 BOTTLE, PLASTIC | LIQUID | 29.6 | 51 | |
| 0283-0569-72 | HurriCaineTopical Anesthetic Liquid | 72 g in 1 APPLICATOR | LIQUID | 72 | 51 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0283-0569-31 | ML - Milliliter | 0283-0569 | 1326f189-9c69-460f-a071-c36eae179397 | 1 | 2012-07-24 |
| 0283-0569-72 | EA - Each | 0283-0569 | 0e9c6d99-ad67-4acf-8ed5-6b7b6f579675 | 1 | 2016-09-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZOCAINE | ACTIVE INGREDIENT | U3RSY48JW5 | HURRICAINE TOPICAL ANESTHETIC LIQUID (BENZOCAINE) LIQUID [BEUTLICH PHARMACEUTICALS, LLC] | 6 | |
| BENZOCAINE | ACTIVE MOIETY | U3RSY48JW5 | HURRICAINE TOPICAL ANESTHETIC LIQUID (BENZOCAINE) LIQUID [BEUTLICH PHARMACEUTICALS, LLC] | 6 | |
| Polyethylene Glycol 400 | INACTIVE INGREDIENT | B697894SGQ | HURRICAINE TOPICAL ANESTHETIC LIQUID (BENZOCAINE) LIQUID [BEUTLICH PHARMACEUTICALS, LLC] | 6 | |
| Saccharin Sodium | INACTIVE INGREDIENT | SB8ZUX40TY | HURRICAINE TOPICAL ANESTHETIC LIQUID (BENZOCAINE) LIQUID [BEUTLICH PHARMACEUTICALS, LLC] | 6 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| SENSODYNE Rapid Relief | STANNOUS FLUORIDE | Haleon US Holdings LLC | f9589e7c-c5ca-4465-8d37-47ad6c69249f | 2024-03-06 | Warnings | M022 |
| SENSODYNE Repair and Protect Extra Fresh | STANNOUS FLUORIDE | Haleon US Holdings LLC | 34260c69-d829-46c0-b12a-5136ee073ba1 | 2024-03-06 | Warnings | M022 |
| AQUAFRESH SENSITIVE MAXIMUM STRENGTH | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 76adbccb-0812-4407-a6fc-a57e6f144fbb | 2024-03-05 | Warnings | M022 |
| SENSODYNE Advanced Whitening | POTASSIUM NITRATE | Haleon US Holdings LLC | a06e2549-3c4e-4818-b53e-1dea6828219f | 2024-03-04 | Warnings | M022 |
| Sensodyne Extra Whitening Cool Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | c977f2c4-e0f3-44d2-aa7a-845f0583af3e | 2024-03-04 | Warnings | M022 |
| Sensodyne Natural white | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 911ac7e4-2b92-43d5-af0b-b5f741b088fb | 2024-03-04 | Warnings | M022 |
| Sensodyne Nourish Healthy White | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | aca38560-2fd7-47be-9e93-2abc3214e856 | 2024-03-04 | Warnings | M022 |
| Sensodyne Nourish Gently Soothing | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 5403ab67-532c-4bdf-9b06-07b1866f37f1 | 2024-03-04 | Warnings | M022 |
| SENSODYNE PRONAMEL Active Shield Fresh Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | e8684615-f544-4871-b935-0a0f93639d7d | 2024-03-04 | Warnings | M022 |
| Sensodyne Pronamel Gentle Whitening Fresh Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 3dfa6827-3aae-4f19-93f6-2ded2faf2ddd | 2024-03-04 | Warnings | M022 |
| Made by Dentists Sensitive and Whitening Fresh Mint | POTASSIUM NITRATE, SODIUM FLUORIDE | MADE BY DENTISTS INC | 0d379c26-69ff-4666-9ad5-7618f0bd139f | 2024-02-27 | Warnings | M022 |
| Polident ProPartial | STANNOUS FLUORIDE | Haleon US Holdings LLC | 557eeb32-64f4-41e8-ada4-91bd39ae2920 | 2024-02-07 | Warnings | M022 |
| SENSODYNE PRONAMEL Daily Protection | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | edffce4d-108b-4ffd-9adf-e12cb42ffddd | 2024-01-24 | Warnings | M022 |
| Peppermint Twist | FLUORIDE | Caldwell Health LLC | 4b28cdd1-0dba-42f5-a9e8-06d9e75b2396 | 2024-01-17 | Warnings | M022 |
| The Natural Dentist Groovy Grape | FLUORIDE | Caldwell Consumer Health LLC | 087abbed-1f58-4b45-a76b-a950fa81c18c | 2024-01-16 | Warnings | M022 |
| Benzoin Tincture | BENZOIN RESIN | Pharma Nobis, LLC | e42fccc2-1b4f-e7f3-e053-2a95a90aef39 | 2023-12-26 | Warnings | M022 |
| Sunmark Benzoin Compound Tincture | BENZOIN RESIN | Strategic Sourcing Services LLC | 0c96d810-83dc-47d3-9a75-63a79feaad0a | 2023-12-19 | Warnings | M022 |
| Benzoin Tincture | BENZOIN RESIN | Humco Holding Group, Inc. | b33b5896-673b-498c-8a58-76ece8552f7a | 2023-12-15 | Warnings | M022 |
| Povidone Iodine | POVIDONE IODINE ORAL RINSE 0.5% | Humco Holding Group, Inc. | b83dbdd1-ff63-caf8-e053-2a95a90a5764 | 2023-12-15 | Warnings | M022 |
| Moon Whitening Gel Anticavity | SODIUM FLUORIDE | Moon Oral Care, LLC | 0c556a29-a697-3a66-e063-6394a90abfee | 2023-12-12 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | PSN | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 808062 | HurriCaine Oral Anesthetic 20 % Mucous Membrane Topical Solution | PSN | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 808062 | benzocaine 200 MG/ML Mucous Membrane Topical Solution [Hurricaine] | SBD | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 308657 | benzocaine 200 MG/ML Mucous Membrane Topical Solution | SCD | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 308657 | benzocaine 20 % Mucous Membrane Topical Solution | SY | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 808062 | Hurricaine 20 % Mucous Membrane Topical Solution | SY | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
| 808062 | Hurricaine 200 MG/ML Mucous Membrane Topical Solution | SY | fee9969d-ad1a-4f44-9741-a0a44c9e1128 | 51 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0283-0569-02 | 00283056902 | 2 g in 1 APPLICATOR (0283-0569-02) | 2 g | 1969-05-15 | 0000-00-00 | No | No | Current |
| 0283-0569-17 | 00283056917 | 1 g in 1 PACKET (0283-0569-17) | 1 g | 2020-01-28 | 0000-00-00 | No | No | Current |
| 0283-0569-31 | 00283056931 | 29.6 g in 1 BOTTLE, PLASTIC (0283-0569-31) | 29.6 g | 1969-05-15 | 0000-00-00 | No | No | Current |
| 0283-0569-72 | 00283056972 | 72 g in 1 APPLICATOR (0283-0569-72) | 72 g | 1969-05-15 | 0000-00-00 | No | No | Current |