MOISTURIZING SUNSCREEN SPF15
- Product NDC
- 59663-001
- 11-digit product format
- 596630001
- Labeler code
- 59663
- Product ID
- 59663-001_887b89ab-92bf-4bfa-b6b3-73539f94255c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OXYBENZONE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Shine & Pretty (USA), Corp.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1996-02-02
- Marketing end
- 0000-00-00
- Substance
- OXYBENZONE; OCTINOXATE
- Active strength
- 1 mL/100mL; mL/200mL
- 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 |
|---|
| 59663-001-01 | MOISTURIZING SUNSCREEN SPF15 | 100 mL in 1 BOTTLE | LOTION | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59663-001 | MOISTURIZING SUNSCREEN SPF15 (OXYBENZONE) LOTION [SHINE & PRETTY (USA), CORP.] | 1 | Legacy NDC, 1 package rows | 20111216_3a0b9ac4-12c0-4ef9-a4e1-56c2ea21dc49.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 59663-001-01 | 59663000101 | 100 mL in 1 BOTTLE | 100 ml | Historical |