Sunscreen
- Product NDC
- 11822-0714
- Requested package NDC
- 11822-0714-3
- 11-digit product format
- 118220714
- Labeler code
- 11822
- Product ID
- 11822-0714_b164a3fe-4df6-4bc3-90b7-f03aab024e1c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Rite Aid
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-12-02
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0714 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [RITE AID] | 5 | Legacy NDC | 20240927_a9f9ca00-47ba-4aa5-9bf9-7a01daba88b4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0714-3 | 11822071403 | 236 mL in 1 BOTTLE, PLASTIC (11822-0714-3) | 236 ml | 2021-12-02 | 0000-00-00 | No | No | Current |