ADVANCED PROTECTION SUNSCREEN SPF-30
- Product NDC
- 70712-101
- 11-digit product format
- 707120101
- Labeler code
- 70712
- Product ID
- 70712-101_de9b12a7-2849-0cb7-e053-2995a90a3456
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OCTISALATE, ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- BOTANICAL SCIENCE, INC.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-07
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; ZINC OXIDE
- Active strength
- 8 g/100mL; g/100mL; g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | 70712-101 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 70712-101 | 70712-101-11 | 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 |
|---|---|---|---|---|---|---|---|---|
| 70712-101-11 | 70712010111 | 100 mL in 1 BOTTLE (70712-101-11) | 100 ml | 2017-08-07 | 0000-00-00 | No | No | Current |