NDC 10157-1007-01 - Stridex Sensitive
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 10157-1007
- Requested NDC
- 10157-1007-01
- Package NDCs from labels
- 10157-1007-1, 10157-1007-2, 10157-1007-3, 10157-1007-4, 10157-1007-01
- Manufacturer
- Blistex Inc
- Effective date
- 2024-12-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Stridex Sensitive - Blistex Inc | Blistex Inc | 2024-12-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10157-1007-1 | Stridex Sensitive | 1 in 1 CARTON | LIQUID | 1 | 3 | |
| 10157-1007-1 | Stridex Sensitive | 55 in 1 JAR | LIQUID | 55 | 3 | |
| 10157-1007-2 | Stridex Sensitive | 1 in 1 CARTON | LIQUID | 1 | 3 | |
| 10157-1007-2 | Stridex Sensitive | 70 in 1 JAR | LIQUID | 70 | 3 | |
| 10157-1007-3 | Stridex Sensitive | 90 in 1 JAR | LIQUID | 90 | 3 | |
| 10157-1007-3 | Stridex Sensitive | 1 in 1 CARTON | LIQUID | 1 | 3 | |
| 10157-1007-4 | Stridex Sensitive | 1 in 1 CARTON | LIQUID | 1 | 3 | |
| 10157-1007-4 | Stridex Sensitive | 110 in 1 JAR | LIQUID | 110 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10157-1007 | STRIDEX SENSITIVE (SALICYLIC ACID) LIQUID [BLISTEX INC] | 3 | Current NDC, Legacy NDC, 8 package rows | 20241215_843d3424-bd6c-44aa-976b-63c9da15014e.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 10157-1007-1 | EA - Each | 10157-1007 | 330a1a5d-859e-45d2-ba0a-b4b56c6e0924 | 1 | 2016-02-04 |
| 10157-1007-2 | EA - Each | 10157-1007 | c865aa9b-a970-4f43-a08c-e9186338f989 | 1 | 2016-02-04 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| OVERNIGHT RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 2c6c4737-dff3-6382-e063-6294a90a412c | 2026-05-14 | Warnings | L7T10EIP3A |
| Pain Relief | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 3ed34e65-9d74-daff-e063-6394a90a94c7 | 2026-05-14 | Warnings | L7T10EIP3A |
| MENTHOL PAIN RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 0e6a09cc-7986-f851-e063-6294a90aff67 | 2026-05-14 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Patch | LIDOCAINE AND MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 3c166165-2ad8-206f-e063-6294a90a52fc | 2026-05-14 | Warnings | L7T10EIP3A |
| OVERNIGHT RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f1041b25-eb09-e43d-e053-2995a90a073a | 2026-05-14 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Patch | LIDOCAINE AND MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f1047707-3fe5-06bc-e053-2995a90a59b9 | 2026-05-14 | Warnings | L7T10EIP3A |
| Elastic Relief Strip | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f103cf8a-a285-28d1-e053-2995a90ae70e | 2026-05-14 | Warnings | L7T10EIP3A |
| Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Toner | SALICYLIC ACID | L'Oreal USA Products Inc | a2dc3cf4-23d2-4cb7-8fdc-615420db5710 | 2026-05-14 | Warnings | M006 O414PZ4LPZ |
| Halls Honey Lemon | MENTHOL | Mondelez Global LLC | aec46410-ffb1-4db4-b232-82110c562f69 | 2026-05-13 | Warnings | L7T10EIP3A |
| Wart Remover Patches | SALICYLIC ACID | Guangzhou Hechuang Commercial Service Co.,Ltd. | 51b385fe-7abc-839d-e063-6394a90a79fc | 2026-05-13 | Warnings | O414PZ4LPZ |
| Pain Relief Gel-Roll On | MENTHOL | Trifecta Pharmaceuticals USA | 51b403dc-fc9b-0cad-e063-6394a90af081 | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 5edddb99-6596-4a3b-b361-1cc04d032c31 | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 684faf63-5e44-4471-8384-e8fa7c0d842a | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 4c798b06-6ee5-41d1-8a14-f6889512ade3 | 2026-05-13 | Warnings | L7T10EIP3A |
| BIOFREEZE | MENTHOL | Reckitt Benckiser LLC | 83d5c2f2-2413-4d28-83b2-0808d0917b4d | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 10a8face-47da-ebbe-e063-6294a90a42fe | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze Foot Cream | MENTHOL | Reckitt Benckiser LLC | 32450cbf-4ed4-402b-a30e-e08a17bba3fb | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | a227213b-e89f-7144-e053-2a95a90a7e74 | 2026-05-13 | Warnings | L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 00bb462a-27d0-6f74-e063-6394a90a90ec | 2026-05-13 | Warnings | L7T10EIP3A |
| BioFreeze Dry Stick | MENTHOL | Reckitt Benckiser LLC | 26d62cd2-9209-8cca-e063-6394a90a2028 | 2026-05-13 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.