SUNSCREEN
- Product NDC
- 55910-877
- 11-digit product format
- 559100877
- Labeler code
- 55910
- Product ID
- 55910-877_4c107ae8-fbfd-0833-e063-6394a90a88cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalat, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Old East Main Co.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-11-15
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 150; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SUNSCREEN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 150 mg/mL |
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55910-877-21 | SUNSCREEN | 88 mL in 1 BOTTLE, PLASTIC | LOTION | 88 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55910-877 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALAT, OCTOCRYLENE) LOTION [OLD EAST MAIN CO.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20241012_db876d34-1af9-4e0a-9e9a-32a8b00e9405.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-877-21 | 55910087721 | 88 mL in 1 BOTTLE, PLASTIC (55910-877-21) | 88 ml | 2019-11-15 | 0000-00-00 | No | No | Current |