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 |
|---|---|---|---|---|---|---|
| SYNC ICE | SYNC RELIEF ICE | iON Pharma, LLC | 38ce98ce-a7bf-8041-e063-6394a90ae730 | 2025-07-28 | Warnings | M017 |
| SYNC PRO | SYNC RELIEF PRO CREAM | iON Pharma, LLC | 3a3e91d6-732b-dca9-e063-6394a90a06d4 | 2025-07-28 | Warnings | M017 |
| Careland Pain Relief | METHYL SALICYLATE, MENTHOL | Planet (Anhui) Pharmaceutical Co., Ltd. | 83f36771-1033-4fd0-a0e6-82c1dcfedeee | 2025-07-28 | Warnings | M017 |
| Rite Aid anti-itch | HYDROCORTISONE | Rite Aid Corporation | 2a232dd1-9071-4c55-a7f7-19d8404b99a6 | 2025-07-28 | Warnings | M017 |
| Hydrocortisone Plus 12 Moisturizers | HYDROCORTISONE | RITE AID CORPORATION | 05598255-3e7a-46a5-ae7e-dcfcb616d59d | 2025-07-28 | Warnings | M017 |
| Inked Inspired | LIDOCAINE HCL | Prodigy Media Inc | 54fb2860-7e63-4598-953a-170226e613e9 | 2025-07-28 | Warnings | M017 |
| Ujhay Hydrocortisone Ointment. | UJHAY HYDROCORTISONE OINTMENT | Guangdong Quadrant Ecological Technology Co., Ltd. | 3af59276-8e6a-0603-e063-6394a90a1f9b | 2025-07-27 | Warnings | M017 |
| SANA SANA Menthol External Analgesic | MENTHOL | Alquimia Najulam S de RL de CV | 8b7edd51-e08a-4e01-9df0-8305ce17b418 | 2025-07-25 | Warnings | M017 |
| Hydrocortisone Intensive Healing Formula | HYDROCORTISONE | TARGET Corporation | 682b737f-e453-4079-bf31-47a9485c7897 | 2025-07-25 | Warnings | M017 |
| Chigg Away | BENZOCAINE | Pierson Laboratories, Inc. | 8372e7c1-f145-4bc5-85ab-cf831abe70ce | 2025-07-24 | Warnings | M017 |
| Chigg Away | BENZOCAINE | Pharma Nobis, LLC | e42fa1c6-d804-630f-e053-2995a90add6b | 2025-07-24 | Warnings | M017 |
| Cannarelief 2000mg | MENTHOL | Earthmed LLC | 01f810de-52ba-8beb-e063-6394a90a61c0 | 2025-07-24 | Warnings | M017 |
| CHING WAN HUNG SOOTHING HERBAL BALM | MENTHOL | TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD. | ffadc904-8e9d-4cb8-815a-d583bbdb3f0b | 2025-07-24 | Warnings | M017 |
| PT Elite Premium Pain Relief | CAPSAICIN, MENTHOL | PT ELITE PRODUCTS LLC | ad251821-4c58-425d-bdcb-8dd9bd41b713 | 2025-07-23 | Warnings | M017 |
| Whipped Butter SPF 50 | ZINC OXIDE | Bloomeffects, Inc | 374b62d8-e012-591f-e063-6294a90aef93 | 2025-07-23 | Warnings | M017 |
| Game On Xtreme | MENTHOL, UNSPECIFIED FORM | Natural Essentials Inc. | 5a1b6192-d537-42b3-add8-22c63e7c986c | 2025-07-23 | Warnings | M017 |
| AMRUTANJAN RELIEF PAIN BALM | CAMPHOR , MENTHOL, METHYL SALICYLATE | AMRUTANJAN HEALTH CARE LIMITED | ddee6714-8b18-4d87-944b-8467fda22e6b | 2025-07-23 | Warnings | M017 |
| Stopain Extra Strength Gel | MENTHOL | Troy Manufacturing, Inc. | 8bb89002-d7a2-4bee-b5a5-1fd1949273ef | 2025-07-22 | Warnings | M017 |
| Hielo Ardiente | MENTHOL | Menper Distributors, Inc. | 97ec516c-d2bc-47ce-82fe-bd68445d9570 | 2025-07-22 | Warnings | M017 |
| La Flecha Japonesa | METHYL SALICYLATE | Menper Distributors, Inc. | 08819ad0-97c2-49bd-b923-535b94a27167 | 2025-07-22 | 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 |