4x Medicated Severe Toothache and Gum Gel
- Product NDC
- 79481-0610
- 11-digit product format
- 794810610
- Labeler code
- 79481
- Product ID
- 79481-0610_437fd357-4fcb-b91b-e063-6394a90a2f3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- GEL
- Route
- ORAL
- Labeler
- Meijer
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-11-20
- Substance
- BENZALKONIUM CHLORIDE; BENZOCAINE; ZINC CHLORIDE; MENTHOL
- Active strength
- .13; 20; .15; .5 g/100g; g/100g; g/100g; g/100g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 79481-0610 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… | ||
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 79481-0610 | 79481-0610-9 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… |
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
- 4x Medicated Severe Toothache and Gum Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | .13 g/100g |
| BENZOCAINE | 20 g/100g |
| ZINC CHLORIDE | .15 g/100g |
| MENTHOL | .5 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5UM2KM3W7 | Internal UNII lookup |
| U3RSY48JW5 | Internal UNII lookup |
| 86Q357L16B | Internal UNII lookup |
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2369638 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 97ce7890-5093-1763-e053-2a95a90afae7 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 362d7abb-94e6-4c60-9a58-266894157713 | Product name | 1 | 20231023 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
| d723478e-ad4a-ec23-6bd7-cfe33e1e3840 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0610-9 | 4x Medicated Severe Toothache and Gum Gel | 7 g in 1 TUBE | GEL | 7 | 5 | |
| 79481-0610-9 | 4x Medicated Severe Toothache and Gum Gel | 1 in 1 CARTON | GEL | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0610 | 4X MEDICATED SEVERE TOOTHACHE AND GUM GEL (BENZALKONIUM CHLORIDE) GEL [MEIJER] | 3 | Current NDC, 2 package rows | 20250119_97ce7890-5093-1763-e053-2a95a90afae7.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 |
|---|---|---|---|---|---|---|
| LenzaPro Flex | LIDOCAINE/MENTHOL | SOLA Pharmaceuticals | ba498f1d-460b-f4e6-e053-2995a90a5755 | 2025-12-08 | Warnings | M017 |
| LidaFlex | LIDOCAINE | SOLA Pharmaceuticals | b9e49529-13b4-1b0b-e053-2995a90adc7a | 2025-12-08 | Warnings | M017 |
| Rugby Menthol Hot Cold Patch | MENTHOL | RUGBY LABORATORIES | c68d29c2-9b56-4994-e053-2a95a90ae60e | 2025-12-08 | Warnings | M017 |
| Neuracin Topical Gel | NEURACIN TOPICAL ANALGESIC GEL | SOLA Pharmaceuticals | c3166926-30c2-2128-e053-2a95a90a0bf2 | 2025-12-08 | Warnings | M017 |
| Triceptin | LIDOCAINE / MENTHOL / METHYL SALICYLATE | SOLA Pharmaceuticals | ef1b98ab-d2db-038c-e053-2995a90a94b4 | 2025-12-08 | Warnings | M017 |
| SynoFlex Patch | SYNOFLEX PATCH | Sola Pharmaceuticals | de2042c4-6c5e-7365-e053-2a95a90ada2a | 2025-12-08 | Warnings | M017 |
| AROAMAS COT NICOTINE TRANSDERMAL PATCHES STEP 1 | NICOTINE TRANSDERMAL PATCHES | PCHEERY LLC | 457c860b-091d-8350-e063-6294a90a2f98 | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP | MENTHOL, CAMPHOR | AY BENDITO INTERNATIONAL, INC | 457c9bd6-2e72-03e5-e063-6394a90a558c | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP ROLL-ON | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 3e552afc-9305-8825-e063-6294a90a1afe | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 457d89aa-4a84-94a6-e063-6294a90a20c0 | 2025-12-08 | Warnings | M017 |
| Gold Bond Medicated Anti-Itch | PRAMOXINE HYDROCHLORIDE, MENTHOL | Gold Bond Co LLC | 4a2bd277-47dd-4ae6-9b4b-e0ae9aad226b | 2025-12-05 | Warnings | M017 |
| Orajel for Cold Sores Double Medicated, Cream | BENZOCAINE AND WHITE PETROLATUM | Church & Dwight Co., Inc. | b8699a40-8464-ca02-e053-2995a90a4260 | 2025-12-05 | Warnings | M017 |
| Thompson Hydrocortisone 1% | HYDROCORTISONE | Thompson | f8740314-7e1f-815e-e053-6294a90a6eae | 2025-12-05 | Warnings | M017 |
| JUST CBD SOOTHING UNSCENTED | LIDOCAINE HCL | Just Brands LLC | 453f44e2-9e5b-8695-e063-6394a90a4389 | 2025-12-05 | Warnings | M017 |
| JUST CBD ROLL-ON COOLING | MENTHOL | Just Brands LLC | 453fa1a7-368c-ae50-e063-6294a90a5507 | 2025-12-05 | Warnings | M017 |
| JUST CBD ROLL-ON WARMING | CAMPHOR | Just Brands LLC | 4540221f-cf9f-9b6a-e063-6294a90adec3 | 2025-12-05 | Warnings | M017 |
| Gold Bond Extra Strength | MENTHOL | Gold Bond Co LLC | 3e84375f-95d3-420c-b222-02a757412592 | 2025-12-04 | Warnings | M017 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | b3ec09b9-7511-0895-e053-2a95a90a7840 | 2025-12-04 | Warnings | M017 |
| Gold Bond Medicated Pain and Itch Relief | LIDOCAINE HYDROCHLORIDE | Gold Bond Co LLC | d240e9b8-3506-42ab-8a50-05e8d3fac4ff | 2025-12-04 | Warnings | M017 |
| BLT Skin Cream | BENZOCAINE, LIDOCAINE, TETRACAINE | M2B Pharma LLC | 9dc5db9d-9e0a-cd28-e053-2995a90a6bf7 | 2025-12-04 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2369638 | benzalkonium chloride 0.13 % / benzocaine 20 % / menthol 0.5 % / zinc chloride 0.15 % Oral Gel | PSN | 97ce7890-5093-1763-e053-2a95a90afae7 | 5 |
| 2369638 | benzalkonium chloride 0.0013 MG/MG / benzocaine 0.2 MG/MG / menthol 0.005 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel | SCD | 97ce7890-5093-1763-e053-2a95a90afae7 | 5 |
| 2369638 | benzalkonium chloride 0.13 % / benzocaine 20 % / menthol 0.5 % / zinc chloride 0.15 % Oral Gel | SY | 97ce7890-5093-1763-e053-2a95a90afae7 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 79481-0610-9 | 79481061009 | 1 TUBE in 1 CARTON (79481-0610-9) / 7 g in 1 TUBE | 1 tube | 2019-11-20 | No | No | Current |