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 |
|---|---|---|---|---|---|---|
| Restoral | MENTHOL | Saje Natural Business Inc. | 5b6176c1-9ed9-1950-e053-2a91aa0a434e | 2026-01-13 | Warnings | L7T10EIP3A |
| END-ZIT | SULFUR | ABBE Laboratories, Inc. | afed5e8e-324c-44c6-abf6-72938376a4b2 | 2026-01-13 | Warnings | M006 |
| Capzasin Quick Relief | CAPSAICIN AND MENTHOL | Chattem, Inc. | d6c313a3-8dc6-4231-95b6-ac9399e1c1be | 2026-01-13 | Warnings | L7T10EIP3A |
| Neutrogena Oil Free Acne Wash | SALICYLIC ACID | Kenvue Brands LLC | c4775032-9723-4208-8a42-145f2b4da1c8 | 2026-01-12 | Warnings | M006 O414PZ4LPZ |
| LONAZEM | MENTHOL,PETROLATUM | PEER PHARM LTD. | 91f7a741-4178-4639-9cd5-746a4b9a21bf | 2026-01-12 | Warnings | L7T10EIP3A |
| BHA CLEANSER 2% | SALICYLIC ACID | Skinfix, Inc. | ceccb599-ff9e-fc87-e053-2a95a90a411a | 2026-01-12 | Warnings | M006 O414PZ4LPZ |
| ACNE SPOT TREATMENT 2% BHA | SALICYLIC ACID | Skinfix, Inc. | ceccea68-07d8-0903-e053-2995a90ab2b7 | 2026-01-12 | Warnings | M006 O414PZ4LPZ |
| Sulfo lo | SULFUR 3% SOAP BAR | Crown Laboratories | 89577417-76a0-cb04-e053-2995a90a5733 | 2026-01-12 | Warnings | M006 |
| Mineral Ice Pain Relieving | MENTHOL | Crown Laboratories | 7b30076a-0af6-2f74-e053-2a91aa0ae08d | 2026-01-12 | Warnings | L7T10EIP3A |
| PanOxyl | BENZOYL PEROXIDE | Crown Laboratories | 1660f219-e789-91f1-e063-6294a90a7664 | 2026-01-12 | Warnings | M006 |
| PanOxyl | BENZOYL PEROXIDE | Crown Laboratories | ff09cbab-304b-4da9-e053-6394a90ae600 | 2026-01-12 | Warnings | M006 |
| PanOxyl Clarifying Exfoliant | SALICYLIC ACID | Crown Laboratories, Inc. | faa6576c-2af2-d86b-e053-6294a90ada2d | 2026-01-12 | Warnings | M006 O414PZ4LPZ |
| PanOxyl | BENZOYL PEROXIDE | Crown Laboratories | 7b301b94-3cc8-b05b-e053-2991aa0aa561 | 2026-01-12 | Warnings | M006 |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | L7T10EIP3A |
| PanOxyl Acne Gel Wash | SALICYLIC ACID | Crown Laboratories, Inc. | 39712bb8-3d4e-29b3-e063-6394a90a95b8 | 2026-01-12 | Warnings | M006 O414PZ4LPZ |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | L7T10EIP3A |
| Solidago | SOLIDAGO VIRGAUREA, UVA-URSI, PAREIRA BRAVA, SABAL SERRULATA, POPULUS TREMULOIDES, STAPHYSAGRIA, CANTHARIS, TEREBINTHIA, BORAX | Marco Pharma International LLC. | 915727a5-78d9-4865-ad35-8a10cce014ca | 2026-01-12 | Warnings | 91MBZ8H3QO |
| Extra Strength Balm | CAPSICUM AND MENTHOL | Saje Natural Business Inc | f516e416-446b-8f21-e053-2a95a90afd88 | 2026-01-12 | Warnings | L7T10EIP3A |
| Pain Release | MENTHOL | Saje Natural Business Inc. | 3df0e56a-7651-42dc-8ed8-f68836a63c61 | 2026-01-12 | Warnings | L7T10EIP3A |
| Trauma Less | MENTHOL | Saje Natural Business Inc. | 650cba4c-6aba-48c3-9c41-841f19905548 | 2026-01-12 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.