SEAWEED BATH CO. SPF 50 SPORT
- Product NDC
- 81159-131
- 11-digit product format
- 811590131
- Labeler code
- 81159
- Product ID
- 81159-131_09e25fad-8fe9-b0f7-e063-6294a90a20e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTOCRYLENE, ZINC OXIDE, OCTISALATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- The Seaweed Bath Co.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-11-23
- Substance
- OCTISALATE; OCTOCRYLENE; ZINC OXIDE
- Active strength
- 50; 100; 85 mg/mL; mg/mL; mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SEAWEED BATH CO. SPF 50 SPORT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 100 mg/mL |
| ZINC OXIDE | 85 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4X49Y0596W, 5A68WGF6WM, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81159-131-00 | SEAWEED BATH CO. SPF 50 SPORT | 100 mL in 1 TUBE | LOTION | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81159-131 | SEAWEED BATH CO. SPF 50 SPORT (OCTOCRYLENE, ZINC OXIDE, OCTISALATE) LOTION [THE SEAWEED BATH CO.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231112_f01516bf-8aed-4402-a3f9-ef11c54d46b3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81159-131-00 | 81159013100 | 100 mL in 1 TUBE (81159-131-00) | 100 ml | 2020-11-23 | 0000-00-00 | No | No | Current |