Stridex XL Face and Body Pads
- Product NDC
- 10157-2114
- 11-digit product format
- 101572114
- Labeler code
- 10157
- Product ID
- 10157-2114_2d206763-baa2-4d21-aa28-008b84dcaf05
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Blistex Inc
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-20
- Substance
- SALICYLIC ACID
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stridex XL Face and Body Pads
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 797892, 1425554 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10157-2114-1 | Stridex XL Face and Body Pads | 90 in 1 JAR | LIQUID | 90 | | 3 |
| 10157-2114-1 | Stridex XL Face and Body Pads | 1 in 1 CARTON | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10157-2114 | STRIDEX XL FACE AND BODY PADS (SALICYLIC ACID) LIQUID [BLISTEX INC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241215_ed459e80-22cc-40ef-862c-1adf82da2377.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10157-2114-1 | 10157211401 | 1 JAR in 1 CARTON (10157-2114-1) / 90 APPLICATOR in 1 JAR / 2 mL in 1 APPLICATOR | 1 jar | 2020-09-20 | 0000-00-00 | No | No | Current |