Camo CC SPF 30 Light 250 W
- Product NDC
- 76354-865
- Requested package NDC
- 76354-865-01
- 11-digit product format
- 763540865
- Labeler code
- 76354
- Product ID
- 76354-865_c77cc924-17ea-09e3-e053-2995a90ad95a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- J.A. Cosmetics U.S. Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-08-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 75 mg/g; mg/g; mg/g
- 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 package | package | 76354-865 | 76354-865-01 | 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 |
|---|---|---|---|---|---|---|---|---|
| 76354-865-01 | 76354086501 | 1 BOTTLE in 1 BOX (76354-865-01) > 30 g in 1 BOTTLE | 1 bottle | 2021-08-01 | 0000-00-00 | No | No | Current |