Sunplus SPF50 Face Body Sunscreen
- Product NDC
- 65112-304
- 11-digit product format
- 651120304
- Labeler code
- 65112
- Product ID
- 65112-304_4a08871f-25e4-215d-e063-6394a90ab8a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- I.Shay Cosmetics
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-06-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- .02; .15; .05; .06 g/118mL; g/118mL; g/118mL; g/118mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunplus SPF50 Face Body Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTOCRYLENE | .02 g/118mL |
| OCTISALATE | .15 g/118mL |
| AVOBENZONE | .05 g/118mL |
| HOMOSALATE | .06 g/118mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5A68WGF6WM, 4X49Y0596W, G63QQF2NOX, V06SV4M95S |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65112-304-01 | Sunplus SPF50 Face Body Sunscreen | 118 mL in 1 TUBE | LOTION | 118 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65112-304 | SUNPLUS SPF50 FACE BODY SUNSCREEN (SUNSCREEN) LOTION [I.SHAY COSMETICS] | 1 | Current NDC, 1 package rows | 20241115_26d55baf-66dc-b1b8-e063-6394a90a670d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 65112-304-01 | 65112030401 | 118 mL in 1 TUBE (65112-304-01) | 118 ml | 2004-06-01 | No | No | Historical |