Hydraday
- Product NDC
- 61220-001
- 11-digit product format
- 612200001
- Labeler code
- 61220
- Product ID
- 61220-001_bda2c93f-6b1f-4827-b6c6-e7572142c1f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octocrylene and Avobenzone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- PF Invest Company
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-11-20
- Marketing end
- 0000-00-00
- Substance
- OCTOCRYLENE; AVOBENZONE
- Active strength
- 3 mg/50mg; mg/50mg
- 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 |
|---|
| 61220-001-01 | Hydraday | 50 mg in 1 PACKAGE | CREAM | 50 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61220-001 | HYDRADAY (OCTOCRYLENE AND AVOBENZONE) CREAM [PF INVEST COMPANY] | 2 | Legacy NDC, 1 package rows | 20131121_98a75101-28ab-4eef-9b4c-b5a6aa8a193c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 61220-001-01 | 61220000101 | 50 mg in 1 PACKAGE | 50 mg | Historical |