Sun Bum SPF 50 Premium Moisturizing Sunscreen
- Product NDC
- 69039-219
- 11-digit product format
- 690390219
- Labeler code
- 69039
- Product ID
- 69039-219_d72eac9b-f192-864f-e053-2995a90a1b08
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Sun Bum, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-26
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 69039-219-01 | Sun Bum SPF 50 Premium Moisturizing Sunscreen | 177 mL in 1 TUBE | LOTION | 177 | | 4 |
| 69039-219-01 | Sun Bum SPF 50 Premium Moisturizing Sunscreen | 1 in 1 BOX | LOTION | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69039-219 | SUN BUM SPF 50 PREMIUM MOISTURIZING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUN BUM, LLC] | 4 | Legacy NDC, 2 package rows | 20220205_da989a2f-d40b-4309-9ae0-14891e624560.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69039-219-01 | 69039021901 | 1 TUBE in 1 BOX (69039-219-01) > 177 mL in 1 TUBE | 1 tube | 2017-08-26 | 0000-00-00 | No | No | Current |