NATURAL SUN AQ SUPER WHITE SUN
- Product NDC
- 51523-022
- 11-digit product format
- 515230022
- Labeler code
- 51523
- Product ID
- 51523-022_4c2ad6f4-78e0-4d04-83d2-67011e511480
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- THEFACESHOP CO., LTD.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-04-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE
- Active strength
- 1 mL/50mL
- 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 |
|---|
| 51523-022-01 | NATURAL SUN AQ SUPER WHITE SUNSPF50 PA | 50 mL in 1 CARTON | CREAM | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51523-022 | NATURAL SUN AQ SUPER WHITE SUN SPF50 PA (TITANIUM DIOXIDE) CREAM [THEFACESHOP CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20100715_f9e48ab7-6d60-41a0-94c6-f5c25ce971cc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51523-022-01 | 51523002201 | 50 mL in 1 CARTON | 50 ml | Historical |