AN ADC FACE UP SPECIAL PROGRAM
- Product NDC
- 69153-020
- 11-digit product format
- 691530020
- Labeler code
- 69153
- Product ID
- 69153-020_14071c01-e34f-403a-9507-03617782ad7a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OATMEAL
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- AN Co Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-08-01
- Marketing end
- 0000-00-00
- Substance
- OATMEAL
- Active strength
- 0 mg/101
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69153-020-01 | AN ADC FACE UP SPECIAL PROGRAM | 10 in 1 CARTON | SOLUTION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69153-020 | AN ADC FACE UP SPECIAL PROGRAM (OATMEAL) SOLUTION [AN CO LTD.] | 1 | Legacy NDC, 1 package rows | 20140926_ae97e7e4-8c9f-4aa3-9515-ae0037721f98.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69153-020-01 | 69153002001 | 10 in 1 CARTON | Historical |