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 |
|---|---|---|---|---|---|---|
| Nufabrx Medicine Infused Socks | CAPSAICIN | Nufabrx LLC | 00d7d5bf-ee03-e73d-e063-6394a90a5d94 | 2025-10-15 | Warnings | M017 |
| Nufabrx Medicine Infused Elbow Sleeve | CAPSAICIN | Nufabrx LLC | 27ef3ef0-2f98-6672-e063-6294a90aeca4 | 2025-10-15 | Warnings | M017 |
| Nufabrx Medicine Infused Wrist Sleeve | CAPSAICIN | Nufabrx LLC | 22572cf9-fc0c-d327-e063-6394a90a2186 | 2025-10-15 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | WALGREENS | eff77965-dc7f-49af-e053-2995a90a1a97 | 2025-10-14 | Warnings | M017 |
| Pleasure Balm Kama Sutra | BENZOCAINE | Cosmetic Enterprises Ltd | f370e3c4-65ca-4f3c-a5aa-70e198e681a2 | 2025-10-14 | Warnings | M017 |
| Vanicream HC Anti-Itch | HYDROCORTISONE | Pharmaceutical Specialties, Inc. | 28b06507-27a5-2cb1-e054-00144ff8d46c | 2025-10-14 | Warnings | M017 |
| Trilogel | LIDOCAINE HYDROCHLORIDE | Trifluent Pharma LLC | 22af7d63-6a56-4a38-a95b-0f88410b23cb | 2025-10-14 | Warnings | M017 |
| PROINNATE Numbing Cream | MENTHOL | Guangzhou Haishi Biological Technology Co., Ltd. | 40c63645-8ed3-82b3-e063-6294a90a5267 | 2025-10-13 | Warnings | M017 |
| Cramergesic | MENTHOL, METHYL SALICYLATE | The Hygenic Company, LLC | d0ffde7a-6942-74fc-e053-2a95a90a484a | 2025-10-13 | Warnings | M017 |
| Tricylate | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Trifluent Pharma LLC | 4869b63a-e01e-4a79-a493-7a1b4d3e914b | 2025-10-13 | Warnings | M017 |
| Doloflex Pain Relief | MENTHOL, METHYL SALICYLATE | United Health & Beauty Corp | 32a830cc-04d3-102e-e063-6294a90a1cad | 2025-10-12 | Warnings | M017 |
| Lidocaine Pain Relieving Gel-Patch | LIDOCAINE | Nanjing Anxing Medical Technology Co., Ltd. | 40c9b132-57ce-865e-e063-6394a90a2080 | 2025-10-10 | Warnings | M017 |
| Kinesys | ZINC OXIDE | Wilc Healthcare Inc | a32b44c3-eda0-48ea-95fc-250a2c2396ca | 2025-10-10 | Warnings | M017 |
| Te-Fu Recovery Massage | MENTHOL, METHYL SALICYLATE | Wasatch Product Development | 7bc2989f-dfb6-e8af-e053-2991aa0a0bf2 | 2025-10-10 | Warnings | M017 |
| Anti-itch | HYDROCORTISONE | Medline Industries, LP | b0947381-c0db-4253-ab40-3d45603ae65d | 2025-10-09 | Warnings | M017 |
| Kalaya Pain Relief | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | e2452c4b-2548-497f-828b-5d960402522a | 2025-10-08 | Warnings | M017 |
| Kalaya Pain Relief 6X with Arnica | PAIN RELIEF CREAM | Avaria Health & Beauty Corp | 60198d2e-4de3-3fa0-e053-2a91aa0afaf7 | 2025-10-08 | Warnings | M017 |
| KALAYA PAIN RELIEF 6X WITH ARNICA - Pain Relief | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | 9b9b7cad-a5e2-4445-856b-4aa439d77a80 | 2025-10-08 | Warnings | M017 |
| KALAYA FOAMING PAIN RELIEF | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | d5021e6d-f29f-446b-874c-bdcabd9cf4f6 | 2025-10-08 | Warnings | M017 |
| KALAYA EXTRA STRENGTH FOAMING PAIN RELIEF | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | e0c9f22a-165a-4558-ba3c-8592f1bd0016 | 2025-10-08 | 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 |