Suntan Lotion
- Product NDC
- 49852-201
- 11-digit product format
- 498520201
- Labeler code
- 49852
- Product ID
- 49852-201_45b4245a-efad-4b1d-b924-fe5fdf36bbc6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE OXYBENZONE TITANIUM DIOXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Tri-Coastal Design Company Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-02-28
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 7 mL/100mL; mL/100mL; mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 49852-201-60 | Suntan Lotion | 60 mL in 1 TUBE | LOTION | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49852-201 | SUNTAN LOTION (OCTINOXATE OXYBENZONE TITANIUM DIOXIDE) LOTION [TRI-COASTAL DESIGN COMPANY INC. ] | 1 | Legacy NDC, 1 package rows | 20100228_68b71261-a795-4df1-b3ee-a165adf4bd89.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49852-201-60 | 49852020160 | 60 mL in 1 TUBE | 60 ml | Historical |