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 |
|---|---|---|---|---|---|---|
| LenzaPro Flex | LIDOCAINE/MENTHOL | SOLA Pharmaceuticals | ba498f1d-460b-f4e6-e053-2995a90a5755 | 2025-12-08 | Warnings | M017 |
| LidaFlex | LIDOCAINE | SOLA Pharmaceuticals | b9e49529-13b4-1b0b-e053-2995a90adc7a | 2025-12-08 | Warnings | M017 |
| Rugby Menthol Hot Cold Patch | MENTHOL | RUGBY LABORATORIES | c68d29c2-9b56-4994-e053-2a95a90ae60e | 2025-12-08 | Warnings | M017 |
| Neuracin Topical Gel | NEURACIN TOPICAL ANALGESIC GEL | SOLA Pharmaceuticals | c3166926-30c2-2128-e053-2a95a90a0bf2 | 2025-12-08 | Warnings | M017 |
| Triceptin | LIDOCAINE / MENTHOL / METHYL SALICYLATE | SOLA Pharmaceuticals | ef1b98ab-d2db-038c-e053-2995a90a94b4 | 2025-12-08 | Warnings | M017 |
| SynoFlex Patch | SYNOFLEX PATCH | Sola Pharmaceuticals | de2042c4-6c5e-7365-e053-2a95a90ada2a | 2025-12-08 | Warnings | M017 |
| AROAMAS COT NICOTINE TRANSDERMAL PATCHES STEP 1 | NICOTINE TRANSDERMAL PATCHES | PCHEERY LLC | 457c860b-091d-8350-e063-6294a90a2f98 | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP | MENTHOL, CAMPHOR | AY BENDITO INTERNATIONAL, INC | 457c9bd6-2e72-03e5-e063-6394a90a558c | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP ROLL-ON | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 3e552afc-9305-8825-e063-6294a90a1afe | 2025-12-08 | Warnings | M017 |
| AY BENDITO HEMP | CAMPHOR, MENTHOL | AY BENDITO INTERNATIONAL, INC | 457d89aa-4a84-94a6-e063-6294a90a20c0 | 2025-12-08 | Warnings | M017 |
| Gold Bond Medicated Anti-Itch | PRAMOXINE HYDROCHLORIDE, MENTHOL | Gold Bond Co LLC | 4a2bd277-47dd-4ae6-9b4b-e0ae9aad226b | 2025-12-05 | Warnings | M017 |
| Orajel for Cold Sores Double Medicated, Cream | BENZOCAINE AND WHITE PETROLATUM | Church & Dwight Co., Inc. | b8699a40-8464-ca02-e053-2995a90a4260 | 2025-12-05 | Warnings | M017 |
| Thompson Hydrocortisone 1% | HYDROCORTISONE | Thompson | f8740314-7e1f-815e-e053-6294a90a6eae | 2025-12-05 | Warnings | M017 |
| JUST CBD SOOTHING UNSCENTED | LIDOCAINE HCL | Just Brands LLC | 453f44e2-9e5b-8695-e063-6394a90a4389 | 2025-12-05 | Warnings | M017 |
| JUST CBD ROLL-ON COOLING | MENTHOL | Just Brands LLC | 453fa1a7-368c-ae50-e063-6294a90a5507 | 2025-12-05 | Warnings | M017 |
| JUST CBD ROLL-ON WARMING | CAMPHOR | Just Brands LLC | 4540221f-cf9f-9b6a-e063-6294a90adec3 | 2025-12-05 | Warnings | M017 |
| Gold Bond Extra Strength | MENTHOL | Gold Bond Co LLC | 3e84375f-95d3-420c-b222-02a757412592 | 2025-12-04 | Warnings | M017 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | b3ec09b9-7511-0895-e053-2a95a90a7840 | 2025-12-04 | Warnings | M017 |
| Gold Bond Medicated Pain and Itch Relief | LIDOCAINE HYDROCHLORIDE | Gold Bond Co LLC | d240e9b8-3506-42ab-8a50-05e8d3fac4ff | 2025-12-04 | Warnings | M017 |
| BLT Skin Cream | BENZOCAINE, LIDOCAINE, TETRACAINE | M2B Pharma LLC | 9dc5db9d-9e0a-cd28-e053-2995a90a6bf7 | 2025-12-04 | 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 |