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 |
|---|---|---|---|---|---|---|
| BLT 2 | LIDOCAINE HCL | CENTURA PHARMACEUTICALS INC | 41dc85ec-d79b-0a32-e054-00144ff8d46c | 2026-01-12 | Warnings | M017 |
| Mineral Ice Pain Relieving | MENTHOL | Crown Laboratories | 7b30076a-0af6-2f74-e053-2a91aa0ae08d | 2026-01-12 | Warnings | M017 |
| Sarna | PRAMOXINE HYDROCHLORIDE | Crown Laboratories | 19b0ce1b-e147-01a1-e063-6394a90af808 | 2026-01-12 | Warnings | M017 |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | M017 |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | HY-VEE, INC | 48350b54-8d9a-48c4-e063-6394a90ac040 | 2026-01-12 | Warnings | M017 |
| LidoPlus Pain Relief | LIDOCAINE HYDROCHLORIDE | Centura Pharmaceuticals, Inc | 07bacc6c-60a6-4297-8663-904a22bdc040 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f2277e27-868b-57ef-e053-2a95a90abf28 | 2026-01-12 | Warnings | M017 |
| BLT 3 | TETRACAINE | CENTURA PHARMACEUTICALS INC | 401a0d22-1181-02ac-e054-00144ff88e88 | 2026-01-12 | Warnings | M017 |
| Sting Relief Prep Pad | BENZOCAINE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 0c901f64-6890-45c0-9ca7-ee9de87903c4 | 2026-01-12 | Warnings | M017 |
| Goodsense Oral Pain Relief | BENZOCAINE | Geiss, Destin and Dunn, Inc. | eb461b70-d10f-4e11-8374-e43713f3504d | 2026-01-12 | Warnings | M017 |
| Extra Strength Balm | CAPSICUM AND MENTHOL | Saje Natural Business Inc | f516e416-446b-8f21-e053-2a95a90afd88 | 2026-01-12 | Warnings | M017 |
| Pain Release | MENTHOL | Saje Natural Business Inc. | 3df0e56a-7651-42dc-8ed8-f68836a63c61 | 2026-01-12 | Warnings | M017 |
| Trauma Less | MENTHOL | Saje Natural Business Inc. | 650cba4c-6aba-48c3-9c41-841f19905548 | 2026-01-12 | Warnings | M017 |
| Mamisan | LIDOCAINE HYDROCHLORIDE, MENTHOL | Miramar Cosmetics, Inc DBA Miramar Lab | 4402e900-c6e9-4f32-8cc4-c84014384a9f | 2026-01-12 | Warnings | M017 |
| Curist Lidocaine Patch | LIDOCAINE 4% PATCH | Little Pharma, Inc. | 1a8fe44e-7a21-c2ab-e063-6394a90a6100 | 2026-01-11 | Warnings | M017 |
| DG Health Pain Relieving | LIDOCAINE HCL | DOLGENCORP, LLC | 923aeb4c-049f-4ecc-a77e-9ffa0e236d4e | 2026-01-11 | Warnings | M017 |
| Campho-Phenique Antiseptic | CAMPHOR (SYNTHETIC) AND PHENOL | Foundation Consumer Healthcare | 46b84e0b-78a9-4cde-9f90-e165b5419162 | 2026-01-09 | Warnings | M017 |
| MyDerm Pro Freeze Cooling Menthol Pain Relief Roll-On | MENTHOL | Inspec Solutions | 12ff9b9a-73e5-ce31-e063-6294a90aeaf8 | 2026-01-09 | Warnings | M017 |
| Carmex Classic Lip Balm Medicated | CAMPHOR (SYNTHETIC), WHITE PETROLATUM | Carma Laboratories, Inc. | bb0278c9-eaff-d435-e053-2995a90a202a | 2026-01-09 | 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 |