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 |
|---|---|---|---|---|---|---|
| Nighttime 4X Medicated Cream | BENZOCAINE | Rite Aid | 21645ed1-2dc0-223a-e063-6394a90ab021 | 2025-11-21 | Warnings | M017 |
| 4x Medicated Gum Cream | BENZOCAINE | Albertsons | b81a308c-9c30-0e3d-e053-2a95a90a15d2 | 2025-11-21 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | b0edd9d9-951f-d3dd-e053-2995a90a8d5a | 2025-11-21 | Warnings | M017 |
| Up up | LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES | Target Corporation | 44121d40-86e1-0df6-e063-6294a90aedaf | 2025-11-20 | Warnings | M017 |
| Up up | PAIN RELIEF ADVANCED HYDROGEL PATCHES | Target Corporation | 44128b70-3172-ee37-e063-6294a90a705f | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | f03090fa-f7e6-f53a-e053-2a95a90aa819 | 2025-11-20 | Warnings | M017 |
| HEATING PAIN RELIEF | METHYL SALICYLATE, MENTHOL | SUNSET NOVELTIES, INC | ff073e47-3107-e17e-e053-6294a90a58fa | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | fc8a8f20-97ab-481e-e053-6394a90a3525 | 2025-11-20 | Warnings | M017 |
| MENTHOL | MENTHOL | SUNSET PAIN RELIEF ROLL-ON 3OZ | 934d4638-b47b-187d-e053-2995a90ae69d | 2025-11-20 | Warnings | M017 |
| FOOT PAIN RELIEF ROLL-ON | LIDOCAINE, MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 43edcea0-ab04-f368-e063-6294a90a817a | 2025-11-19 | Warnings | M017 |
| Absolut Skin Corticosoothe Anti-Itch | HYDROCORTISONE | Absolut Skin Incorporated | deb52218-9176-4aaa-a22f-b66dada6690f | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy | LIDOCAINE | InterMed Laboratories Private Limited | 43f3d189-f6b7-02ed-e063-6394a90afd73 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch HealthA2Z | LIDOCAINE | InterMed Laboratories Private Limited | 43f3e288-e828-8130-e063-6394a90a6d44 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Leader | LIDOCAINE | InterMed Laboratories Private Limited | 42f06914-c8b8-ea9c-e063-6294a90a79e6 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | CAMPHOR, MENTHOL | CVS | 87715662-c788-9a8d-e053-2a95a90acb53 | 2025-11-19 | Warnings | M017 |
| Walgreen Anti Itch | CAMPHOR, MENTHOL | Walgreens | b4f47a8d-d4a6-9233-e053-2a95a90afd90 | 2025-11-19 | Warnings | M017 |
| Leader Anti-Itch | CAMPHOR, MENTHOL | LEADER/Cardinal Helath 110, Inc. | 9ca985c6-5017-0558-e053-2995a90a8202 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | PRAMOXINE HCL | CVS | 87fc476a-5b12-7383-e053-2995a90a530b | 2025-11-19 | Warnings | M017 |
| Walgreen Anti-Itch | PRAMOXINE HCL | Walgreens | b5f9d1c5-891e-4377-e053-2995a90aa281 | 2025-11-19 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 89f5f688-856f-f2df-e053-2995a90a73cf | 2025-11-19 | 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 |