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 |
|---|---|---|---|---|---|---|
| Mineral Ice Extreme Dry Stick | MENTHOL | Carlin Consumer Health LLC | 4f81be91-92e5-1205-e063-6394a90a6e82 | 2026-06-02 | Warnings | M017 |
| Kalaya Extra Strength Pain Relief Gel with Arnica | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | b6a6237d-b471-4102-b5df-fc389f5f9258 | 2026-06-02 | Warnings | M017 |
| Biofreeze Ultraflex | LIDOCAINE | Reckitt Benckiser LLC | 2655974b-a67d-9f07-e063-6294a90a54e8 | 2026-06-02 | Warnings | M017 |
| Biofreeze Ultraflex Plus | LIDOCAINE, MENTHOL | Reckitt Benckiser LLC | 401e1843-e9a6-fda9-e063-6294a90a3073 | 2026-06-02 | Warnings | M017 |
| Pain Relief | MENTHOL SPRAY | Owell Naturals Brand, LLC | 534c871c-da35-6135-e063-6294a90aa9f6 | 2026-06-02 | Warnings | M017 |
| Charm Tex FLUORIDE Gel | SODIUM FLUORIDE | Jiangsu Gold Worldworks Household Chemicals Co., Ltd. | 09d47bd7-1438-4ef2-85e0-9cd5eb2f763a | 2026-05-31 | Warnings | M017 |
| Charm Tex FLUORIDE | SODIUM MONOFLUOROPHOSPHATE | Jiangsu Gold Worldworks Household Chemicals Co., Ltd. | 2bddc69a-0c0f-47fc-bc98-90c2ec70dd6f | 2026-05-31 | Warnings | M017 |
| Sting Relief Prep Pad | BENZOCAINE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 9487d15d-9116-4ff8-a004-ba0835ea091e | 2026-05-31 | Warnings | M017 |
| Careland Kinesiology Pain Relieving Tape | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE | Planet (Anhui) Pharmaceutical Co., Ltd. | 35d24cfc-9d34-4fd7-9312-1673b092a3b9 | 2026-05-31 | Warnings | M017 |
| Walgreens Scalp Itch Relief | HYDROCORTISONE | Walgreens | 34952272-1f9e-c642-e063-6394a90ae2bd | 2026-05-29 | Warnings | M017 |
| Aspercreme with Lidocaine No-Mess Applicator | LIDOCAINE HYDROCHLORIDE | Chattem, Inc. | 8092cde7-28d0-4755-b5c0-5765934e572f | 2026-05-29 | Warnings | M017 |
| Belladona and Arnica | MENTHOL | Dannso Corp./d.b.a. Essential Products | fc4e63e4-cebc-49ff-8900-7238261d0fe0 | 2026-05-28 | Warnings | M017 |
| Insect Sting Relief | BENZOCAINE, ALCOHOL | Hubei Fanjian Medical Product Co.,Ltd | f30401c1-961e-44dd-e053-2a95a90a69d6 | 2026-05-28 | Warnings | M017 |
| Menthol plus Camphor Pain Relief | MENTHOL, CAMPHOR | Veridian Healthcare | 4a054949-0889-7182-e063-6394a90aff5e | 2026-05-28 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | CVS Pharmacy | 960bfe55-87f6-3e51-e053-2995a90a867d | 2026-05-27 | Warnings | M017 |
| MyDerm Medical 5 Lidocaine Numbing Roll-On | LIDOCAINE | Inspec Solutions | 1d466be1-a780-462f-8dd4-87478da096aa | 2026-05-27 | Warnings | M017 |
| myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol | MENTHOL | Inspec Solutions LLC. | d427d623-c2fd-7d6b-e053-2995a90abdc3 | 2026-05-27 | Warnings | M017 |
| Caldyphen Clear | PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE | Amerisource Bergen | d8802e56-649e-4494-86ee-7ca8841cc28b | 2026-05-27 | Warnings | M017 |
| Equate Itch Relief Gel | ITCH RELIEF GEL | Walmart, Inc | 7d7bb750-017e-c60e-e053-2991aa0ad671 | 2026-05-26 | Warnings | M017 |
| MyDerm Bite and Sting | BENZOCAINE | Medline Industries | bf45c4dd-5814-4602-b96b-f82a44948763 | 2026-05-26 | 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 |