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 |
|---|---|---|---|---|---|---|
| LIDOGUARD | LIDOCAINE 4% | ViolaCare, Inc. | d8b021b6-cf71-4f7e-9d27-92d0982bd34f | 2026-03-25 | Warnings | M017 |
| LactiGo | MENTHOL | LactiGo, Inc. | 4dda6ac4-d849-69a6-e063-6394a90a3c54 | 2026-03-25 | Warnings | M017 |
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a33f9a9-1fdc-7cdf-e063-6294a90adca1 | 2026-03-25 | Warnings | M017 |
| EjaGuard | LIDOCAINE | MOLANSPACE INC | 475f64ef-d636-7e87-e063-6294a90ae32f | 2026-03-25 | Warnings | M017 |
| Hydrocortisone 1% | HYDROCORTISONE | ProStat First Aid | 4e53d29c-ed3c-f481-e063-6294a90a3181 | 2026-03-25 | Warnings | M017 |
| Topicaine Ultra | TOPICAINE ULTRA | Oncora Pharma, LLC | e052f718-700a-44e0-8770-65451b812ee1 | 2026-03-24 | Warnings | M017 |
| Hot Pap Cataplasma | METHYL SALICYLATE, VANILLYL NONYLAMIDE | Masaem Company | 4dbeda13-b198-0cf0-e063-6294a90a8180 | 2026-03-24 | Warnings | M017 |
| Barmicil Anti-itch | HYDROCORTISONE | OPMX LLC | 850084c3-1dd4-eb8d-e053-2a91aa0a130b | 2026-03-24 | Warnings | M017 |
| Jeil Hangbang Paff Soo S Cataplasma | GLYCOL SALICYLATE, L-MENTHOL | Masaem Company | 4dd040db-07cf-361a-e063-6394a90a8001 | 2026-03-24 | Warnings | M017 |
| Zenol Double Action | METHYL SALICYLATE, L-MENTHOL | BA TRADE INC | 4da998fc-75a3-583f-e063-6394a90a59c7 | 2026-03-23 | Warnings | M017 |
| Ultra Strength Topical Pain Relief Cream | CAMPHOR, MENTHOL, METHYL SALICYLATE | J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD | 4db9ae57-4ab4-8fe4-e063-6394a90a7e51 | 2026-03-23 | Warnings | M017 |
| DR. SANA ALIVIO TOTAL ALIVIO TOTAL ROLL ON | ALIVIO TOTAL ROLL ON | EVI LABS | 4da01338-8739-08a8-e063-6294a90ae157 | 2026-03-22 | Warnings | M017 |
| DR SANA ALIVIO TOTAL ALIVIO TOTAL | ALIVIO TOTAL | EVI LABS | 4da1c3b8-9af2-6e9f-e063-6394a90a86ae | 2026-03-22 | Warnings | M017 |
| SORE NO MORE | MENTHOL CAMPHOR | SOMBRA COSMETICS INC. | 80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd | 2026-03-20 | Warnings | M017 |
| CVS Health Antiseptic Wound Wash | LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE | CVS Pharmacy | 53ac017a-eccb-3b24-e054-00144ff88e88 | 2026-03-20 | Warnings | M017 |
| Tecnu Diphenhydramine HCl Pain Relieving Anti Itch Gel 2% | ANTI ITCH GEL | Walgreens | 3d6e8c62-2fcc-51c2-e063-6394a90a33f7 | 2026-03-20 | Warnings | M017 |
| ANIXIKE Numbing | MENTHOL 5% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4d5c52d7-8e81-b62f-e063-6394a90ad03e | 2026-03-19 | Warnings | M017 |
| SYLVIRENE NUMBING | MENTHOL 5% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4d47e8c7-d293-bf63-e063-6294a90a5fd9 | 2026-03-18 | Warnings | M017 |
| Antibiotic and Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | STRATEGIC SOURCING SERVICES LLC | f7aa9330-c47c-4d2f-b784-11b831d919d6 | 2026-03-18 | Warnings | M017 |
| hydrocortisone | HYDROCORTISONE | Bryant Ranch Prepack | 99726aa3-3b45-4175-8471-279419af5457 | 2026-03-18 | 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 |