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 |
|---|---|---|---|---|---|---|
| ACD A | CITRIC ACID MONOHYDRATE, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE | Terumo BCT, Ltd | 8e255bc7-a120-460a-a32d-43931f8115de | 2026-05-21 | Warnings, Adverse reactions | 2968PHW8QP |
| LidoPro Patch | LIDOCAINE, MENTHOL, AND METHYL SALICYLATE | Preferred Pharmaceuticals Inc. | 6c9a076e-6316-427b-9ce6-c8fe2d388837 | 2026-05-21 | Warnings | L7T10EIP3A |
| EVEN KEEL RESURFACING PEEL | SALICYLIC ACID | Personal Day Inc. | 330dd564-ebac-46f0-8c2a-34bbf60887d1 | 2026-05-20 | Warnings | M006 O414PZ4LPZ |
| DAILY SELF DISCOVERY SET | SALICYLIC ACID | Personal Day Inc. | 93c7a610-8282-49a9-9128-0f92a92abaa7 | 2026-05-20 | Warnings | M006 |
| DOING THE WORK SALICYLIC ACID ACNE TREATMENT | SALICYLIC ACID | Personal Day Inc. | 4193a9ab-686a-494e-ade7-6e900e47e5b6 | 2026-05-20 | Warnings | M006 O414PZ4LPZ |
| Antispetic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Rockland Cosmetics, Inc. | 1bbae739-5e54-64cb-e063-6294a90a3745 | 2026-05-20 | Warnings, Adverse reactions | L7T10EIP3A |
| Antiseptic Mouthrinse | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Rockland Cosmetics, Inc. | b7c63ae5-08a8-436a-bbaa-f3ab3c2a5e67 | 2026-05-20 | Warnings, Adverse reactions | L7T10EIP3A |
| WHITENING SUNSCREENANTI WRINKLE | WHITENING SUNSCREENANTI WRINKLE | Shantou Oushiya Biotechnology Co.,Ltd | 524384e9-b3f8-4c13-e063-6394a90a8973 | 2026-05-20 | Warnings | 059QF0KO0R |
| Biofreeze Triple Target Roll-On | CAMPHOR, CAPSAICIN, MENTHOL | Reckitt Benckiser LLC | 5089c088-3026-233a-e063-6394a90a93b6 | 2026-05-19 | Warnings | L7T10EIP3A |
| CeraVe Developed with Dermatologists BHA Exfoliating Toner Acne Treatment | SALICYLIC ACID | L'Oreal USA Products Inc | 434ab915-faa3-40a7-8f8d-ff0eeef95e1f | 2026-05-19 | Warnings | M006 O414PZ4LPZ |
| Tobaccotox | AVENA SATIVA, KALI PHOSPHORICUM, CACTUS GRANDIFLORUS, EUCALYPTUS GLOBULUS, LOBELIA INFLATA, DAPHNE INDICA, MENTHOLUM, IGNATIA AMARA, NUX VOMICA, STAPHYSAGRIA, TABACUM, BENZINUM, NAPHTHALINUM | BioActive Nutritional, Inc. | b286c7fd-e456-49bf-bb82-0fd32eeb3723 | 2026-05-18 | Warnings | L7T10EIP3A |
| MORKORIA BEE VENOM WART REMOVER | SALICYLIC ACID 17% BEE VENOM 1% BEE VENOM WART REMOVER | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a1e3a7a-0570-a95f-e063-6394a90adbc7 | 2026-05-18 | Warnings | O414PZ4LPZ |
| Salicylic acid | CALLUS REMOVERS | Premier Brands of America Inc. | 0b637f58-5604-454d-99ba-24115113ac3d | 2026-05-18 | Warnings | O414PZ4LPZ |
| Skin Tag Remove | SKIN TAG REMOVE | Shenzhen Earth Surface Trading Co., Ltd. | 5224362c-967e-9b98-e063-6294a90a9867 | 2026-05-18 | Warnings | O414PZ4LPZ |
| Blistex Maximum Hydration Lip | CAMPHOR (SYNTHETIC), DIMETHICONE, UNSPECIFIED, MENTHOL, UNSPECIFIED FORM, AND PHENOL | Blistex Inc. | fed223bc-edf3-46eb-b678-acb906f9ef11 | 2026-05-18 | Warnings | L7T10EIP3A |
| Tiger Balm | CAMPHOR (SYNTHETIC), MENTHOL, AND CAPSICUM | Haw Par Healthcare Ltd. | 5066dc10-e4d5-49e9-9a5f-0ac220cfbf28 | 2026-05-18 | Warnings | L7T10EIP3A |
| Menthol Overnight Pain Relief Gel-Patch | MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 104fad7b-d95f-f8e3-e063-6294a90a65fc | 2026-05-17 | Warnings | L7T10EIP3A |
| Pain Relief Gel-Patch | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 0ae6cfd1-bbea-3fe6-e063-6294a90a541f | 2026-05-17 | Warnings | L7T10EIP3A |
| Menthol Pain Relief Gel-Patch | MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 0ae7af3a-7dfc-9736-e063-6394a90abe3c | 2026-05-17 | Warnings | L7T10EIP3A |
| Pain Relief Gel-Patch | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 32e1df3a-2f8f-68df-e063-6294a90aa1d1 | 2026-05-17 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.