FOOTSPA PEDI
- Product NDC
- 49283-707
- 11-digit product format
- 492830707
- Labeler code
- 49283
- Product ID
- 49283-707_4318c0bb-2dca-29a7-e063-6394a90ac2ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- CHEMCO CORPORATION
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-17
- Marketing end
- 2027-12-31
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- 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 | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49283-707-16 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49283-707-04 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49283-707-01 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49283-707-16 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49283-707-04 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49283-707-01 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49283-707-16 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49283-707-04 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49283-707-01 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49283-707-16 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49283-707-04 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49283-707-01 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49283-707-16 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49283-707-04 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49283-707-01 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49283-707-04 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49283-707-01 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 49283-707-16 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49283-707-04 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49283-707-01 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 49283-707-16 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49283-707-04 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49283-707-01 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 49283-707-16 | U | Excluded because listing certification expired | 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
- FOOTSPA PEDI
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 70 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1041849 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 04de4392-74f6-7df8-e063-6294a90ae3b1 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 49283-707-01 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-01 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-04 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-04 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-16 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-16 | 2025-11-08 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-01 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-01 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-04 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-04 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-16 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
| 49283-707-16 | 2025-01-30 | 49283-707-16 49283-707-04 49283-707-01 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49283-707-01 | FOOTSPA PEDI | 3785 mL in 1 BOTTLE | SPRAY | 3785 | 2 | |
| 49283-707-04 | FOOTSPA PEDI | 118 mL in 1 BOTTLE, SPRAY | SPRAY | 118 | 2 | |
| 49283-707-16 | FOOTSPA PEDI | 473 mL in 1 BOTTLE, SPRAY | SPRAY | 473 | 2 |
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 |
|---|---|---|---|---|---|---|
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35ac19-6883-a733-e063-6294a90ad22d | 2024-11-05 | Warnings | M017 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products, Inc. | cfe8114b-df65-064b-e053-2a95a90a33f6 | 2024-11-05 | Warnings | M017 |
| Alocane Botanicals | LIDOCAINE HYDROCHLORIDE | Quest Products, LLC. | 02a8e5c7-56f4-eb0d-e063-6294a90a80cd | 2024-11-05 | Warnings | M017 |
| Alocane Emergency Burn Pads | LIDOCAINE HYDROCHLORIDE | Quest Products, Inc. | fe58bb89-7216-4121-afd3-d1438bdfbfa2 | 2024-11-05 | Warnings | M017 |
| Licefreee AfterLice | PRAMOXINE HCI | Tec Laboratories Inc. | 06c4cc42-a215-3949-e063-6394a90a665e | 2024-11-05 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | ASO LLC | cb9505b7-222d-3a24-e053-2a95a90a0b64 | 2024-11-05 | Warnings | M017 |
| TopCare Pain Relieving Analgesic | LIDOCAINE HYDROCHLORIDE | Topco Associates LLC | 6b4783e0-1987-4838-9e8c-b95426d62b28 | 2024-11-05 | Warnings | M017 |
| Eagle Green Balm | CAMPHOR MENTHOL | Borden Company (Private) Limited | 6f7a796b-a31c-0e60-e053-2a91aa0a022b | 2024-11-04 | Warnings | M017 |
| Muscular Balm | CAPSAICIN MENTHOL METHYL SALICYLATE | Borden Company (Private) Limited | ed79f14e-6b3d-4bf2-9c34-d019c1ba2582 | 2024-11-04 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE | A-S Medication Solutions | 3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e3 | 2024-11-04 | Warnings | M017 |
| Walgreens Ice Blue Pain Relieving Topical Analgesic | MENTHOL, UNSPECIFIED FORM | Walgreen Company | 1c0ee442-ffd2-4f6c-aab2-f70e295378ad | 2024-11-04 | Warnings | M017 |
| Walgreen Cool n Heat Maximum Strength Pain Relieving | MENTHOL, UNSPECIFIED FORM | Walgreen Company | d5c79476-dde8-4a85-8878-bc2ac3a3d70b | 2024-11-04 | Warnings | M017 |
| LIDOCAINE | LIDOCAINE | STRATUS PHARMACEUTICALS INC | 87a4f559-a4f6-4b9f-98de-b55b073a11c6 | 2024-11-01 | Warnings | M017 |
| Walgreens Nerve Pain Relieving Topical Analgesic | LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM | Walgreen Company | 83849eca-e02f-4b43-b3a7-b25e987e08a8 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica White | CAMPHOR | Sanvall Enterprises, Inc | 192039a2-aed6-821b-e063-6394a90a7f29 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Reforzada | CAMPHOR | Sanvall Enterprises, Inc | 1921a4b1-cd36-195e-e063-6294a90a8793 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Pain Releiving Roll On with Camphor | CAMPHOR | Sanvall Enterprises, Inc | 173db0e2-611f-55b9-e063-6394a90ac987 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Camphor | CAMPHOR | Sanvall Enterprises, Inc | 1921e851-cf83-0bdb-e063-6294a90a357f | 2024-10-31 | Warnings | M017 |
| cortisone | HYDROCORTISONE | CVS Pharmacy | c766deac-d993-4e48-a5c3-4cfde7338dff | 2024-10-31 | Warnings | M017 |
| Walgreens Pain Relieving with Lavender Analgesic | LIDOCAINE HYDROCHLORIDE | Walgreen Company | 6c7b39c8-5b65-430a-a529-5b6b14adce18 | 2024-10-31 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1041849 | ethanol 70 % Topical Spray | PSN | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2 |
| 1041849 | ethanol 0.7 ML/ML Topical Spray | SCD | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2 |
| 1041849 | ethanol 70 % Topical Spray | SY | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49283-707-01 | 49283070701 | 3785 mL in 1 BOTTLE (49283-707-01) | 3785 ml | 2023-09-08 | 2027-12-31 | No | No | Historical |
| 49283-707-04 | 49283070704 | 118 mL in 1 BOTTLE, SPRAY (49283-707-04) | 118 ml | 2023-09-08 | 2027-12-31 | No | No | Historical |
| 49283-707-16 | 49283070716 | 473 mL in 1 BOTTLE, SPRAY (49283-707-16) | 473 ml | 2023-09-08 | 2027-12-31 | No | No | Historical |