DAYCLING
- Product NDC
- 71816-0001
- 11-digit product format
- 718160001
- Labeler code
- 71816
- Product ID
- 71816-0001_5c42f15b-d624-bede-e053-2991aa0a0084
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- magnesium stearate
- Dosage form
- TABLET
- Route
- VAGINAL
- Labeler
- ISTK3
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-10-24
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM STEARATE
- Active strength
- 5 mg/1
- 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 |
|---|
| 71816-0001-1 | DAYCLING | 6 in 1 BLISTER PACK | TABLET | 6 | | 1 |
| 71816-0001-1 | DAYCLING | 2 in 1 CARTON | TABLET | 2 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71816-0001 | DAYCLING (MAGNESIUM STEARATE) TABLET [ISTK3] | 1 | Legacy NDC, 2 package rows | 20171024_5c42f15b-d623-bede-e053-2991aa0a0084.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 71816-0001-1 | 71816000101 | 6 in 1 BLISTER PACK | Historical |