sunscreen
- Product NDC
- 72036-938
- Requested package NDC
- 72036-938-14
- 11-digit product format
- 720360938
- Labeler code
- 72036
- Product ID
- 72036-938_c27faae8-414e-4425-b92d-5ed42a69c3aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Harris Teeter
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-07-18
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 90 g/g; g/g; g/g; g/g
- 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 package | package | 72036-938 | 72036-938-14 | 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 |
|---|---|---|---|---|---|---|---|---|
| 72036-938-14 | 72036093814 | 156 g in 1 BOTTLE, SPRAY (72036-938-14) | 156 g | 2020-07-18 | 0000-00-00 | No | No | Current |