Formo Cresol
- Product NDC
- 0699-0412
- 11-digit product format
- 006990412
- Labeler code
- 0699
- Product ID
- 0699-0412_b2917c26-a3fc-48a9-b5f0-1d62fe15af74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cresol
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- DSHealthcare
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1963-02-19
- Marketing end
- 0000-00-00
- Substance
- CRESOL
- Active strength
- 485 mg/g
- Pharmacologic classes
- Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0699-0412-01 | Formo Cresol | 4292.19 g in 1 BOTTLE, GLASS | LIQUID | 4292.19 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0699-0412 | FORMO CRESOL (CRESOL) LIQUID [DSHEALTHCARE] | 1 | Legacy NDC, 1 package rows | 20100719_6989bddc-910e-47e6-aa8f-619a330e81b8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0699-0412-01 | 00699041201 | 4292.19 g in 1 BOTTLE, GLASS | 4292.19 g | Historical |