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 |
|---|---|---|---|---|---|---|
| Signature Care Menthol | MENTHOL 4% | Safeway | 27d3cb47-a6c7-5b7a-e063-6394a90a056f | 2024-12-05 | Warnings | M017 |
| ITCH X | BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE | BF ASCHER AND CO INC | 03c16d33-8f59-0184-e054-00144ff8d46c | 2024-12-05 | Warnings | M017 |
| PO First Aid Series BURN | LIDOCAINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | f1c349a8-216d-4233-922e-c95329a33d1e | 2024-12-05 | Warnings | M017 |
| Post Treatment Balm | HYDROCORTISONE | Allure Labs Inc. | faa803e6-453c-4d86-85dd-5a5dcdd72d02 | 2024-12-05 | Warnings | M017 |
| CBD Pain Relief Cream | TROLAMINE SALICYLATE | Allure Labs | b6b3102a-4154-2da2-e053-2995a90ae99f | 2024-12-05 | Warnings | M017 |
| CVS Health Pain Relieving | CAMPHOR (SYNTHETIC), MENTHOL (UNSPECIFIED FORM), METHYL SALICYLATE | Natural Essentials, Inc. | f7198485-3d68-41d2-b9b9-f932a0649310 | 2024-12-04 | Warnings | M017 |
| Salonpas LIDOCAINE PLUS | BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE | Hisamitsu America, Inc. | 364924d3-fac3-4f4e-9b40-decd4ec48245 | 2024-12-03 | Warnings | M017 |
| Bite and Itch | DIPHENHYDRAMINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE | Weeks & Leo Co., Inc. | 0a4d471b-c3f3-0a6a-e063-6394a90ad57b | 2024-12-03 | Warnings | M017 |
| Menthol | AMISH ORIGINS MEDICATED | Amish Origins LLC | 547abe39-3af3-4d70-99dd-caf8d67feda2 | 2024-12-03 | Warnings | M017 |
| Meijer Small Cold-Hot Medicated Patches | MENTHOL | Meijer Distribution Inc | be6012d6-2062-45ba-8fc4-abf14cff5845 | 2024-12-03 | Warnings | M017 |
| Salonpas | CAMPHOR, MENTHOL, METHYL SALICYLATE | Hisamitsu Pharmaceutical Co., Inc. | acdd5622-a9a7-4cc3-877e-57efea23303f | 2024-12-03 | Warnings | M017 |
| Salonpas | CAMPHOR, MENTHOL, METHYL SALICYLATE | Hisamitsu Pharmaceutical Co., Inc. | 5bb6c6a3-7dc0-463d-ab2c-9f3bd3f3eff5 | 2024-12-03 | Warnings | M017 |
| Salonpas DEEP Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | Hisamitsu America, Inc. | a4ddb2b9-d023-4c8c-9285-93d51f93207d | 2024-12-03 | Warnings | M017 |
| Salonpas LIDOCAINE PLUS | BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE | Hisamitsu America, Inc. | ea5b4a7f-d47d-4dbd-9288-c01329e387e5 | 2024-12-03 | Warnings | M017 |
| Hempvana Ultra Strength Pain Relief - Overnight | LIDOCAINE | Telebrands Corp | 1030d478-6805-6579-e063-6294a90a0c76 | 2024-12-02 | Warnings | M017 |
| Campho-Phenique Cold Sore Treatment | CAMPHOR (SYNTHETIC) AND PHENOL | Foundation Consumer Healthcare LLC | 106c0bb2-f2e2-4255-867d-d09ff6a5a2e6 | 2024-12-02 | Warnings | M017 |
| Campho-Phenique Antiseptic | CAMPHOR (SYNTHETIC) AND PHENOL | Foundation Consumer Healthcare LLC | 82edaef0-0709-4ae1-a664-c9c5adb91ee1 | 2024-12-02 | Warnings | M017 |
| Thermacare Arthritis and Nerve Pain Therapy Capsaicin Roll On | THERMACARE CAPSAICIN ROLL ON | Clarion Brands LLC | 2850f7e7-41dd-f5f9-e063-6394a90ae519 | 2024-12-02 | Warnings | M017 |
| BURN | LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 2ec1cf79-c341-4b79-9047-ce29f0dff419 | 2024-11-29 | Warnings | M017 |
| TheraCare Pain Relieving Lidocaine Cream | LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | 242204d3-efc7-f7a9-e063-6294a90a5af1 | 2024-11-27 | 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 |