SCANTILY PAD
- Product NDC
- 81953-100
- 11-digit product format
- 819530100
- Labeler code
- 81953
- Product ID
- 81953-100_48c4d99f-9b27-7bf3-e063-6394a90a57ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acne Treatment
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Dermala Inc
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-06-01
- Substance
- SALICYLIC ACID
- Active strength
- .01 mg/mg
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81953-100-01 | SCANTILY PAD | 50 mg in 1 JAR | LIQUID | 50 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81953-100 | SCANTILY PAD (ACNE TREATMENT) LIQUID [DERMALA INC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241212_c5145f1d-78f7-22b4-e053-2a95a90a5c59.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81953-100-01 | 81953010001 | 50 mg in 1 JAR (81953-100-01) | 50 mg | 2021-06-01 | 0000-00-00 | No | No | Current |