MediSpa SunSpray
- Product NDC
- 52554-2001
- 11-digit product format
- 525542001
- Labeler code
- 52554
- Product ID
- 52554-2001_7dd4f01c-7789-46a4-8617-c0782e79ccdf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Universal Cosmetic Co., Ltd
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-08-06
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ENZACAMENE; OCTOCRYLENE
- Active strength
- 0 mL/mL; mL/mL; mL/mL
- 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 |
|---|
| 52554-2001-1 | MediSpa SunSpraysunblock | 55 mL in 1 BOTTLE, WITH APPLICATOR | SPRAY | 55 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52554-2001 | MEDISPA SUNSPRAY SUNBLOCK (OCTINOXATE) SPRAY [UNIVERSAL COSMETIC CO., LTD] | 1 | Legacy NDC, 1 package rows | 20100806_340929aa-6fd8-49e9-932e-b4851caa0b02.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52554-2001-1 | 52554200101 | 55 mL in 1 BOTTLE, WITH APPLICATOR | 55 ml | Historical |