Lincoln
- Product NDC
- 69636-3066
- 11-digit product format
- 696363066
- Labeler code
- 69636
- Product ID
- 69636-3066_45c4d71e-99f9-18ce-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Lincoln Pharmaceuticals Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-10
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 4 g/100g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 69636-3066-4 | Lincoln | 99.2 g in 1 TUBE | CREAM | 99.2 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69636-3066 | LINCOLN (ZINC OXIDE) CREAM [LINCOLN PHARMACEUTICALS LTD.] | 1 | Legacy NDC, 1 package rows | 20170111_45c4d71e-99f8-18ce-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69636-3066-4 | 69636306604 | 99.2 g in 1 TUBE | 99.2 g | Historical |