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 |
|---|---|---|---|---|---|---|
| RELIBONEOintment | TOPICAL ANALGESICOINTMENT | Guangdong Jiaoyu Biotechnology Co., Ltd | 58ddaaf6-18ec-8c5b-e063-6294a90a2828 | 2026-08-12 | Warnings | M017 |
| Capsaicin Cream | CAPSAICIN | Trifecta Pharmaceuticals USA LLC | 58de3a29-2bec-6e44-e063-6394a90a9c1a | 2026-08-12 | Warnings | M017 |
| HYDROCORTISONE | HYDROCORTISONE | Amazon.com Services LLC | f40b4223-e81f-4cd0-bc9b-d3d33ce8cce5 | 2026-08-12 | Warnings | M017 |
| Muscle Rub Cream | MUSCLE RUB | ALLIED TRADE LINK LLC | 11d33e60-8c64-4316-a29a-d17e3e6e4a28 | 2026-08-11 | Warnings | M017 |
| Gee Gason | MALE GENITAL DESENSITIZER | Mon Gars Boutique Inc | 58c75e5c-b801-017f-e063-6394a90a1c75 | 2026-08-11 | Warnings | M017 |
| Capsaicin Cream | CAPSAICIN | Trifecta Pharmaceuticals USA LLC | 58c84330-15bf-c397-e063-6394a90aba05 | 2026-08-11 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE | TARGET Corporation | 4a140b9a-0e3c-4b50-b9c0-9e72616bb7d5 | 2026-08-11 | Warnings | M017 |
| Itch Relief | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE | CVS Pharmacy | 0e988da1-1904-431d-a152-bdb2aacc8e16 | 2026-08-11 | Warnings | M017 |
| Medicated BODY | MENTHOL | CVS Pharmacy, Inc. | a0f61498-69c8-4ce0-bbd7-3a807f192d36 | 2026-08-11 | Warnings | M017 |
| Muscle Move | MENTHOL | Saje Natural Wellness Inc. | 526d3305-4cf8-2fc5-e063-6394a90ad53b | 2026-08-10 | Warnings | M017 |
| Relieve and Relax Pain Relieving | CAMPHOR (SYNTHETIC), MENTHOL | MAC Innovations, LLC | c0528c36-d322-8110-e053-2995a90add6c | 2026-08-08 | Warnings | M017 |
| CVS Pain Relief | MENTHOL | CVS Pharmacy | 4aa629f5-8b8f-cc67-e063-6394a90a019f | 2026-08-07 | Warnings | M017 |
| Instant Cooling Itch Relief | HYDROCORTISONE | CVS Pharmacy | 46545d04-5958-d136-e063-6394a90a3462 | 2026-08-07 | Warnings | M017 |
| CVS Itch Relief | PRAMOXINE HYDROCHLORIDE, ZINC ACETATE | CVS Pharmacy | 46921bea-fcbe-94d6-e063-6394a90a726b | 2026-08-07 | Warnings | M017 |
| CVS Isopropyl Rubbing Alcohol | ISOPROPYL ALCOHOL | CVS Pharmacy | 524605f9-8b04-b600-e063-6394a90a4a02 | 2026-08-07 | Warnings | M017 |
| Lidonex | LIDOCAINE HCL, MENTHOL | Aldama Pharmaceuticals, Inc | 365cf19c-70e0-c4e9-e063-6294a90ac428 | 2026-08-07 | Warnings | M017 |
| Blaster Pain Relief Stick | MENTHOL, METHYL SALICYLATE, CAMPHOR | Kalahari Rose, LLC | 587d660a-5f80-de5a-e063-6394a90aa287 | 2026-08-07 | Warnings | M017 |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | Cardinal Health, 110 dba Leader | 3ed7b8a1-012f-459d-878c-813b93d4673c | 2026-08-06 | Warnings, Adverse reactions | M017 |
| Gel Cooling Pain Relief | MENTHOL | The Kroger Co. | 6fb0acc8-8dab-452c-b09e-de97306e1c32 | 2026-08-06 | Warnings, Adverse reactions | M017 |
| Lidocaine Tattoo Wipe | LIDOCAINE HYDROCHLORIDE | MD Tattoo Company | 369c1d16-597c-e1dc-e063-6394a90a3104 | 2026-08-06 | 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 |