Pharmacys Prescription Vapor Rub
- Product NDC
- 72197-007
- 11-digit product format
- 721970007
- Labeler code
- 72197
- Product ID
- 72197-007_2c69c634-e137-1428-e063-6294a90aa8f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- American Consumer Products Corp
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-09-28
- Substance
- EUCALYPTUS OIL; CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM
- Active strength
- 1; 4.7; 1 g/100g; g/100g; g/100g
- 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 | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 72197-007-04 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 72197-007-04 | 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
- Pharmacys Prescription Vapor Rub
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| EUCALYPTUS OIL | 1 g/100g |
| CAMPHOR (SYNTHETIC) | 4.7 g/100g |
| MENTHOL, UNSPECIFIED FORM | 1 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2R04ONI662 | Internal UNII lookup |
| 5TJD82A1ET | Internal UNII lookup |
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1042788 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6ef328ff-f5c3-515d-e053-2a91aa0a32d3 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72197-007-04 | Pharmacys Prescription Vapor Rub | 110 g in 1 BOTTLE, PLASTIC | GEL | 110 | 4 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Right Remedies Adult Long Lasting Cough Relief Softgel | DEXTROMETHORPHAN HYDROBROMIDE | Strive Pharmaceuticals Inc. | e3ea468e-4e12-4dae-b222-8e32456b77b8 | 2025-01-02 | Warnings | M012 |
| AVON HeXashield Congestion Relief Original | OXYMETAZOLINE HYDROCHLORIDE | Tai Guk Pharm. Co., Ltd. | 8f2c152c-c564-0cba-e053-2a95a90ab3c7 | 2025-01-01 | Warnings | M012 |
| Multi-Symptom Nighttime Cold and Flu Relief | ACETAMINOPHEN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HBR | Advanced Rx LLC | a75553bd-f3f0-47bd-b3c3-aeeb0d1a81b4 | 2025-01-01 | Warnings | M012 |
| Cough Relief | DEXTROMETHORPHAN HYDROBROMIDE | Advanced Rx LLC | 297e10e3-e740-4434-91a2-2e5c54985d33 | 2025-01-01 | Warnings | M012 |
| MUCUS RELIEF DM | GUAIFENESIN, DEXTROMETHORPHAN HBR | Advanced Rx LLC | 64620186-a45b-4c35-a3b9-a347348f93f7 | 2025-01-01 | Warnings | M012 |
| DM Max | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Best Choice | 57a44bbf-a304-47b9-8adc-4442c7787853 | 2025-01-01 | Warnings | M012 |
| Long Acting Cough Softgels | DEXTROMETHORPHAN HYDROBROMIDE | CVS PHARMACY, INC | 322daee6-c61d-43d3-a54d-a354fd3df242 | 2025-01-01 | Warnings | M012 |
| Adult Tussin DM Lil Drug Store Products | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | Lil' Drug Store Products, Inc | 1915cf2a-ebaa-4c47-8991-5b741fa01be2 | 2024-12-31 | Warnings | M012 |
| Congestion Relief Lil Drug Store Products | OXYMETAZOLINE HYDROCHLORIDE | Lil' Drug Store Products, Inc | 8fca348c-ecb6-4a91-89dd-8bd4c05ac745 | 2024-12-31 | Warnings | M012 |
| DAYTIME COLD AND FLU MULTI SYMPTOM | DAYTIME COLD AND FLU MULTI SYMPTOM | TARGET CORP | 9dea350d-2f09-b944-e053-2995a90a2b63 | 2024-12-30 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Walgreens | 2b7aa3f5-3bc9-471f-8ff7-3c52719f0acb | 2024-12-30 | Warnings | M012 |
| Pediacare Childrens Cough and Cold Grape | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | RANDOB LABS,LTD. DBA CROSSINGWELL CONSUMER HEALTH | fabafdc1-9dd8-4258-af49-bab1e29ad109 | 2024-12-30 | Warnings | M012 |
| Pediacare Childrens Cough and Congestion Grape | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | RANDOB LABS,LTD. DBA CROSSINGWELL CONSUMER HEALTH | 9576723b-748c-45e7-bc0d-cc109b9f6735 | 2024-12-30 | Warnings | M012 |
| Cold and Flu Nighttime Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Lil' Drug Store Products, Inc. | ef6836fa-d104-d7b3-e053-2a95a90af2b8 | 2024-12-30 | Warnings | M012 |
| Circle K Congestion Relief | OXYMETAZOLINE HYDROCHLORIDE | Lil' Drug Store Products, Inc | 7e02fe57-f42f-4d3c-9002-4c4c0b1fafd6 | 2024-12-30 | Warnings | M012 |
| SDA Laboratories Tussin | GUAIFENESIN | SDA Laboratories, Inc. | 2a444cc8-96be-9432-e063-6394a90a1b63 | 2024-12-27 | Warnings | M012 |
| SDA Laboratories Tussin DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | SDA Laboratories, Inc. | 2a445f31-818d-11b1-e063-6294a90a8cb1 | 2024-12-27 | Warnings | M012 |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Richmond Pharmaceuticals Inc. | f184b2aa-91a4-44f9-b688-d4e318181984 | 2024-12-26 | Warnings | M012 |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Richmond Pharmaceuticals, Inc. | 2792032a-ff0f-4d5f-a8e3-b8b8c54f4e99 | 2024-12-26 | Warnings | M012 |
| OXYMETAZOLINE HYDROCHLORIDE | OXYMETAZOLINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION INC. | c7b1f980-9b0d-4f63-a70d-fd366658f863 | 2024-12-26 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1042788 | camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel | PSN | 6ef328ff-f5c3-515d-e053-2a91aa0a32d3 | 4 |
| 1042788 | camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical Gel | SCD | 6ef328ff-f5c3-515d-e053-2a91aa0a32d3 | 4 |
| 1042788 | camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel | SY | 6ef328ff-f5c3-515d-e053-2a91aa0a32d3 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72197-007-04 | 72197000704 | 110 g in 1 BOTTLE, PLASTIC (72197-007-04) | 110 g | 2018-09-28 | 0000-00-00 | No | No | Current |