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 |
|---|---|---|---|---|---|---|
| Itch Eraser | DIPHENHYDRAMINE HCL | Tender Corporation d/b/a Adventure Ready Brands | 2204e135-6a23-68a2-e063-6394a90ac019 | 2025-11-18 | Warnings | M017 |
| Analgesic Balm | MENTHOL 10%, METHYL SALICYLATE 15% | Geri-Care Pharmaceuticals, Corp | c8594e10-661f-6ff3-e053-2995a90ab4fc | 2025-11-18 | Warnings | M017 |
| Mag 5 PT Cooling Formula Recovery Cream | MENTHOL | RENU LABORATORIES, LLC | a45cde67-64ec-643b-e053-2a95a90a10b6 | 2025-11-18 | Warnings | M017 |
| After Ivy Wipe | CAMPHOR | Tender Corporation d/b/a Adventure Ready Brands | 21d98018-826a-1d0d-e063-6294a90a0a71 | 2025-11-17 | Warnings | M017 |
| Itch Eraser Gel | DIPHENHYDRAMINE HCL | Tender Corporation d/b/a Adventure Ready Brands | 223c7cfd-6dc5-140a-e063-6394a90a8332 | 2025-11-17 | Warnings | M017 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Kroger Co. | 6b3e7aac-395f-48cf-9c5e-f7e163724aef | 2025-11-17 | Warnings | M017 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | HY-VEE, INC | 415ecfe9-3145-f23e-e063-6394a90adfd8 | 2025-11-17 | Warnings | M017 |
| AY BENDITO - CBD | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 04b1d605-60aa-56f4-e063-6294a90ae760 | 2025-11-17 | Warnings | M017 |
| AY BENDITO - CBD | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 0f1406fe-3a2f-bf36-e063-6294a90a7e5e | 2025-11-17 | Warnings | M017 |
| AY BENDITO CBD | MENTHOL, CAMPHOR | AY BENDITO INTERNATIONAL, INC | 30a1c6b7-e37e-32c2-e063-6394a90aa354 | 2025-11-17 | Warnings | M017 |
| ETERNAL SPIRIT BEAUTY PAINLESS WITH CBD 3000 | MENTHOL, CAMPHOR | Worldwide Cosmetics, Inc | 0816cc8f-8d0b-de27-e063-6294a90a8a9d | 2025-11-17 | Warnings | M017 |
| JUST CBD ROLL-ON COOLING | MENTHOL | Just Brands LLC | f6538e3e-4663-679c-e053-2995a90a87b5 | 2025-11-17 | Warnings | M017 |
| JUST CBD ROLL-ON WARMING | CAMPHOR | Just Brands LLC | f65455d7-04a9-6217-e053-2995a90a7c90 | 2025-11-17 | Warnings | M017 |
| JUST CBD - CBD AND THC ULTRA RELIEF | MENTHOL, CAMPHOR | Just Brands LLC | f664eb79-8897-3a49-e053-2995a90a37b4 | 2025-11-17 | Warnings | M017 |
| JUST CBD RELIEF SOOTHING | LIDOCAINE HCL | Just Brands LLC | f9aff6e7-5702-f61c-e053-6294a90aa66f | 2025-11-17 | Warnings | M017 |
| JUST CBD SOOTHING | MENTHOL, CAMPHOR | Just Brands LLC | 0abece07-976c-4881-e063-6294a90a5c1b | 2025-11-17 | Warnings | M017 |
| Blue-Emu Thrive Pain Relief Cream | TRIPELENNAMINE 0.5% | Kingsway Pharmaceuticals dba NFI, LLC | a4ba6787-c99b-4bf2-9f8f-e923ef976212 | 2025-11-14 | Warnings | M017 |
| CVS Cooling Patch | MENTHOL | CVS Pharmacy | 42d97e29-f32d-a31b-e063-6394a90a88d8 | 2025-11-14 | Warnings | M017 |
| Lidocaine | LIDOCAINE | Marlex Pharmaceuticals Inc | 4de2bc60-dc4a-4417-984f-eabab0e926a6 | 2025-11-14 | Warnings | M017 |
| EXTREME EMU | MENTHOL, METHYL SALICYLATE | Renu Laboratories, LLC | 4393b57b-1e70-b8dd-e063-6294a90ae748 | 2025-11-14 | 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 |