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 |
|---|---|---|---|---|---|---|
| Lidocaine and Menthol | LIDOCAINE AND MENTHOL | Advanced Rx of Tennessee, LLC | 44840250-2112-6ef4-e063-6394a90acdcc | 2026-06-12 | Warnings | M017 |
| DRAWYUM Pain Relief Gel-Patch | LIDOCAINE 4% PAIN RELIEF GEL-PATCH | Jiangxi Yudexi Pharmaceutical Co., LTD | 497e6e18-ba46-0001-e063-6294a90af026 | 2026-06-12 | Warnings | M017 |
| NATUHEAL JOINT BACK PAIN RELIEF | ARNICA MONTANA HPUS 7% JOINT BACK PAIN RELIEF | Jiangxi Yudexi Pharmaceutical Co., LTD | 4c923afa-4d1e-0776-e063-6294a90a2f54 | 2026-06-12 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE CREAM 1% | Aldermed Inc. | 4a7b532e-b292-b595-e063-6394a90acc9c | 2026-06-12 | Warnings | M017 |
| MG PLUS MENTHOL | MENTHOL | RENU LABORATORIES, LLC | 53737365-b985-3800-e063-6294a90a37f2 | 2026-06-11 | Warnings | M017 |
| CeraVe Developed with Dermatologists Itch Relief Moisturizing | PRAMOXINE HYDROCHLORIDE | L'Oreal USA Products Inc | 7c78d980-fc94-498c-aec5-464c0c76c8f4 | 2026-06-11 | Warnings | M017 |
| ANIXIKE Numbing | LIDOCAINE4% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a47f1ed-d8cf-3b0b-e063-6394a90a932a | 2026-06-11 | Warnings | M017 |
| Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride | PRAMOXINE HYDROCHLORIDE | The Honey Pot Company LLC | 81ab7fa7-d9b0-49dc-9782-02f37e588c5e | 2026-06-10 | Warnings | M017 |
| HealthWise Pain Relief Cream with Lidocaine | LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | ef176d33-10b9-ddb2-e053-2995a90a76e3 | 2026-06-10 | Warnings | M017 |
| Warm Patch Tong Gu Huo Luo Gao | PAIN PATCH | Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory | 6906c4a0-1557-45e3-b915-80e4dd652ee7 | 2026-06-10 | Warnings | M017 |
| LidoMedix | LIDOCAINE, MENTHOL, CAMPHOR | Absolute Therapeutics, LLC | 53d504ef-eea3-6a47-e063-6394a90a1f65 | 2026-06-09 | Warnings | M017 |
| good sense anti itch | HYDROCORTISONE | Preferred Pharmaceuticals Inc. | e51047da-8e17-4dd7-be3c-54820a7485f2 | 2026-06-09 | Warnings | M017 |
| Terramed Just Think Comfort GynoCare BV Guard Intimate Wash | PRAMOXINE HYDROCHLORIDE | Rida LLC | 09964550-049c-4c3b-817d-37e660c2e45c | 2026-06-08 | Warnings | M017 |
| Quality Choice Lidocaine Pain Relief Patch | LIDOCAINE | Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) | 526abe69-4bbc-6e73-e063-6394a90ad25d | 2026-06-08 | Warnings | M017 |
| Dcsily Numbing Cream | LIDOCAINE | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 53cab09c-6d5d-471e-e063-6294a90aa977 | 2026-06-08 | Warnings | M017 |
| Easment 0.1% Capsaicin cream for sensitive skin | CAPSAICIN 0.1% | Easment LLC | 537e0106-9e1c-66b8-e063-6294a90ac538 | 2026-06-05 | Warnings | M017 |
| Maximum Strength Pain Relief | MENTHOL CREAM | OWELL NATURALS LLC | 5388f2c5-8cfd-a601-e063-6294a90a2e5f | 2026-06-04 | Warnings | M017 |
| MG PLUS ROLL ON | MENTHOL ROLL ON | RENU LABORATORIES, LLC | 535dc42f-38c7-2afc-e063-6294a90ae23d | 2026-06-03 | Warnings | M017 |
| OP First Aid Series Insect Sting Relief Pad | BENZOCAINE, ISOPROPYL ALCOHOL | Yiwu Ori-Power Medtech Co.,Ltd. | b43af183-834a-0f64-e053-2995a90a3218 | 2026-06-03 | Warnings | M017 |
| PURE PRIMAL DELAY | LIDOCAINE HCL | Prodigy Media Inc | 1ddab664-7c44-452f-854f-e386cd69505e | 2026-06-03 | 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 |