SUNSCREEN
- Product NDC
- 55910-940
- 11-digit product format
- 559100940
- Labeler code
- 55910
- Product ID
- 55910-940_2e234b26-1ebf-4f6e-ba32-f74268e0275b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- OLD EAST MAIN CO
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-07-08
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-940 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [OLD EAST MAIN CO.] | 8 | Legacy NDC | 20241013_75d5fa3b-c1fb-4ba4-baaf-bb714a4d1833.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-940-21 | 55910094021 | 89 mL in 1 CAN (55910-940-21) | 89 ml | 2019-07-08 | 0000-00-00 | No | No | Current |