FACE VALUES ULTRA SPORT ACTIVE SPF 50 SUNSCREEN
- Product NDC
- 63940-068
- 11-digit product format
- 639400068
- Labeler code
- 63940
- Product ID
- 63940-068_c54dd017-805d-3756-e053-2a95a90a733e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- HARMON STORES, INC.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-04-06
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 63940-068 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 63940-068 | 63940-068-09 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63940-068-09 | 63940006809 | 88.7 mL in 1 TUBE (63940-068-09) | 88.7 ml | 2017-04-06 | 0000-00-00 | No | No | Current |