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 |
|---|---|---|---|---|---|---|
| RELISPRAY NATURAL PAIN RELIEF | MENTHOL | Midas-Care Pharmaceuticals, Pvt. Ltd | adc8a43c-19a1-4eb3-9820-b63f7b5e91ea | 2025-10-30 | Warnings | M017 |
| Aveeno Anti-Itch Concentrated | ZINC OXIDE, FERRIC OXIDE RED, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 07f4d4d0-9cee-46c3-bc71-2024abd31c9e | 2025-10-29 | Warnings | M017 |
| zourunan Relieve itching cream ANTIFUNGAL | RELIEVE ITCHING CREAM | Guchutang Biotechnology (Longyan) Co., Ltd | 41bb9ced-dde4-2998-e063-6394a90a8159 | 2025-10-29 | Warnings | M017 |
| zourunan Intensive healing lotion. for ECZEMA | INTENSIVE HEALING LOTION | Guchutang Biotechnology (Longyan) Co., Ltd | 41bad9f3-f1a7-e92c-e063-6394a90ad0ba | 2025-10-29 | Warnings | M017 |
| Aromalief Pain Relief Cream Orange Ginger | MENTHOL | Marketites LLC | 9e8d3611-ef1b-4ac6-e053-2995a90af28a | 2025-10-29 | Warnings | M017 |
| Aromalief Calming Pain Relief Cream Lavender | MENTHOL | Marketites LLC | b8197d52-ccfb-b008-e053-2995a90a0a53 | 2025-10-29 | Warnings | M017 |
| Aromalief Cozy Vanilla Pain Relief Cream | MENTHOL | Marketites LLC | 3634e55e-8c62-a782-e063-6394a90a6508 | 2025-10-29 | Warnings | M017 |
| BENOVA PAIN AND ITCH RELIEF | MENTHOL, 0.11% | BENOVA RX LLC | 42513ee2-8b40-a9f3-e063-6394a90a9386 | 2025-10-29 | Warnings | M017 |
| Burn Relief | LIDOCAINE | CVS Pharmacy | 7e9285fd-26d5-3eac-e053-2991aa0ae2db | 2025-10-29 | Warnings | M017 |
| Coralite Ultra Strength Pain Relief | CAMPHOR MENTHOL | United Exchange Corp. | 44ecf959-cc07-4adc-a500-075b2ee69548 | 2025-10-29 | Warnings | M017 |
| GoodSense Pain Relief | LIDOCAINE | Geiss, Destin & Dunn, Inc | 826f8da4-8468-ea0a-e053-2991aa0a66cb | 2025-10-28 | Warnings | M017 |
| CALMADOL | CAMPHOR, MENTHOL, METHYL SALICYLATE | GRANDALL DISTRIBUTING, LLC | 31b7f84e-8b66-4d31-8e9c-279d0af2fe64 | 2025-10-28 | Warnings | M017 |
| XRay DOL | CAMPHOR, MENTHOL, AND METHYL SALICYLATE | Genomma Lab USA, Inc. | e07fef46-68d9-769c-e053-2a95a90aa065 | 2025-10-28 | Warnings | M017 |
| CVS Medicated Heat | CAPSICUM EXTRACT | CVS Pharmacy | 81cd1019-93a6-311b-e053-2991aa0a7997 | 2025-10-28 | Warnings | M017 |
| Foster and Thrive | LIDOCAINE | STRATEGIC SOURCING SERVICES, LLC | f950b072-d978-b629-e053-6394a90abfaf | 2025-10-28 | Warnings | M017 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Premier Brands of America, Inc. | d3452573-f91f-f157-e053-2a95a90a1ad8 | 2025-10-27 | Warnings | M017 |
| PR | MENTHOL | Amphp, Inc | 6f5b9e08-c445-4fac-e053-2a91aa0aa737 | 2025-10-27 | Warnings | M017 |
| Lidocaine | BURN RELIEF | Foodhold USA | b25dc0df-02d0-41ac-b36c-2c04baa77ef2 | 2025-10-27 | Warnings | M017 |
| Menthol | MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE | FSA Store Inc. | fb3548c8-f202-dc50-e053-6394a90a5b30 | 2025-10-27 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE CONTINUOUS SPRAY | Premier Brands of America, Inc. | d344f68b-9b62-3029-e053-2995a90a1665 | 2025-10-27 | 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 |