Luminess SPF30 Suncreen Setting Powder
- Product NDC
- 73368-150
- Requested package NDC
- 73368-150-18
- 11-digit product format
- 733680150
- Labeler code
- 73368
- Product ID
- 73368-150_a83aefe2-d1e2-432c-e053-2995a90a7d28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide,Titanium Dioxide
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Kinetics Derma Beauty, L.L.C
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-08-01
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 0 g/.15g; g/.15g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | 73368-150 | 73368-150-18 | D | Discontinued by firm | 2026-10-12 |
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 |
|---|---|---|---|---|---|---|---|---|
| 73368-150-18 | 73368015018 | 18 g in 1 CARTON (73368-150-18) | 18 g | 2020-08-01 | 0000-00-00 | No | No | Current |