BEACH DREAM GLITTERY SUNSCREEN
- Product NDC
- 76853-104
- 11-digit product format
- 768530104
- Labeler code
- 76853
- Product ID
- 76853-104_0a7da197-b99b-4dc0-8407-5b524f5fa228
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Block LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-23
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 76853-104-11 | BEACH DREAM GLITTERY SUNSCREENSPF 50 | 90 mL in 1 TUBE | LOTION | 90 | | 2 |
| 76853-104-12 | BEACH DREAM GLITTERY SUNSCREENSPF 50 | 180 mL in 1 TUBE | LOTION | 180 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76853-104 | BEACH DREAM GLITTERY SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BLOCK LLC] | 2 | Legacy NDC, 2 package rows | 20200824_467b65a2-c2d3-43bd-a568-9bec36399055.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76853-104-11 | 76853010411 | 90 mL in 1 TUBE (76853-104-11) | 90 ml | 2020-08-23 | 0000-00-00 | No | No | Current |
| 76853-104-12 | 76853010412 | 180 mL in 1 TUBE (76853-104-12) | 180 ml | 2020-08-23 | 0000-00-00 | No | No | Current |