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 |
|---|---|---|---|---|---|---|
| REINREUDE BACK PAIN THERAPY | CAMPHOR 80MG MENTHOL 24MG BACK PAIN THERAPY | Jiangxi Yudexi Pharmaceutical Co., LTD | 4dfc77bb-11dd-e0f0-e063-6294a90a4e9c | 2026-07-24 | Warnings | M017 |
| DRAVYNOR QUIT SMOKING Patches | NICOTINE18% MENTHOL 0.3% QUIT SMOKING PATCHES | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 5768631f-d517-5b43-e063-6294a90a8f46 | 2026-07-24 | Warnings | M017 |
| DERMFREE NUMBING | LIDOCAINE4% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5b47ce-2bf1-42c7-e063-6294a90af09f | 2026-07-23 | Warnings | M017 |
| DERMFREE WART CORN REMOVER | SALICYLIC ACID 40% WART CORN REMOVER | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5c63b3-44de-8736-e063-6394a90ac21a | 2026-07-23 | Warnings | M017 |
| DERMFREE Anti-itch | HYDROCORTISONE1% ANTI-ITCH | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5af4c6-555a-e74c-e063-6394a90aa6ce | 2026-07-23 | Warnings | M017 |
| DERMFREE HEMORRHOID | LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5d0e79-d620-0147-e063-6294a90a3103 | 2026-07-23 | Warnings | M017 |
| MAG 5 PT WARMING FORMULA | MENTHOL | RENU LABORATORIES, LLC | a499ac9b-0e8e-e23f-e053-2a95a90abe9a | 2026-07-23 | Warnings | M017 |
| Icy Hot Performance Cream Pain Relief | MENTHOL 16%, CAMPHOR 11% | Chattem, Inc. | 73f7a113-ef11-4932-bf4d-4e62863f7941 | 2026-07-23 | Warnings | M017 |
| Numbing Pain Relief | LIDOCAINE 4% | Walgreen Company | 2425badb-e196-e9f8-e063-6294a90a7bf4 | 2026-07-22 | Warnings | M017 |
| Cooling Pain Relief | MENTHOL 4.5% | Walgreen Company | 24345ccf-c96f-31b0-e063-6294a90a82b5 | 2026-07-22 | Warnings | M017 |
| Heat Pain Relief | CAPSAICIN 0.1% | Walgreen Company | 2434f9cf-74aa-17af-e063-6294a90a56d9 | 2026-07-22 | Warnings | M017 |
| Pain Relief Patch Lidocaine | LIDOCAINE | HyVee | 41c26a66-3371-2c2c-e063-6294a90aa38b | 2026-07-22 | Warnings | M017 |
| CVS Ultra Strength Muscle | MENTHOL, CAMPHOR, METHYL SALICYLATE | CVS Pharmacy | 48bef8bc-6e39-a328-e063-6394a90ae450 | 2026-07-22 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | AKRON PHARMA INC | daad9a1e-98d2-4ce7-9d97-ac5d81905abb | 2026-07-22 | Warnings | M017 |
| Professional Therapy MuscleCare Pain Relieving | MENTHOL, CAMPHOR | Active and Innovative | 573c2d85-9e0b-7955-e063-6394a90aff64 | 2026-07-22 | Warnings | M017 |
| DOCTOR INK TOPICAL ANTISEPTIC WITH PAIN RELIEF | BENZALKONIUM CHLORIDE, LIDOCAINE | Enviro Specialty Chemicals Inc | f7abe66c-dc2d-4ef7-9b11-5b87157fd302 | 2026-07-21 | Warnings | M017 |
| Bclsks NUMBING | MENTHOL 1% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 49e26770-ddf6-7515-e063-6394a90a4ab3 | 2026-07-21 | Warnings | M017 |
| Rstrvbr QUIT SMOKING | NICOTINE21MG QUIT SMOKING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5e9691-727f-6bcd-e063-6294a90aadfc | 2026-07-21 | Warnings | M017 |
| Rstrvbr QUIT SMOKING | NICOTINE14MG QUIT SMOKING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5eec19-7f9a-d277-e063-6294a90ace95 | 2026-07-21 | Warnings | M017 |
| Rstrvbr QUIT SMOKING | NICOTINE7MG QUIT SMOKING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a5f124e-2dd7-16b8-e063-6294a90a5cdb | 2026-07-21 | 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 |