Sun Bum Face 50 Premium Sunscreen SPF 50
- Product NDC
- 44717-080
- Requested package NDC
- 44717-080-01
- 11-digit product format
- 447170080
- Labeler code
- 44717
- Product ID
- 44717-080_40d36900-8fdd-17ae-e063-6394a90ab565
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalte, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Wasatch Product Development, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-02-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 10; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sun Bum Face 50 Premium Sunscreen SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| AVOBENZONE | 3 g/100mL |
| HOMOSALATE | 10 g/100mL |
| OCTISALATE | 5 g/100mL |
| OCTOCRYLENE | 10 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| G63QQF2NOX | Internal UNII lookup |
| V06SV4M95S | Internal UNII lookup |
| 4X49Y0596W | Internal UNII lookup |
| 5A68WGF6WM | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| f4ac746a-a50a-8041-e053-2a95a90a8ea6 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44717-080-01 | Sun Bum Face 50 Premium Sunscreen SPF 50 | 88 mL in 1 TUBE | LOTION | 88 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44717-080 | SUN BUM FACE 50 PREMIUM SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALTE, OCTISALATE, OCTOCRYLENE) LOTION [WASATCH PRODUCT DEVELOPMENT, LLC] | 2 | Current NDC, 1 package rows | 20241024_f4ac746a-a50a-8041-e053-2a95a90a8ea6.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357eee3c-1c21-5efb-e063-6294a90a4bb7 | 2025-12-15 | M020 | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357e75ec-473e-df76-e063-6294a90a70c7 | 2025-12-15 | M020 | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357f2f62-904a-2234-e063-6394a90aee72 | 2025-12-15 | M020 | |
| Superscreen Daytime Mineral Sunscreen | ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357f915a-bd77-350b-e063-6294a90ad27f | 2025-12-15 | M020 | |
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357ff025-84ad-6d77-e063-6394a90aad95 | 2025-12-15 | M020 | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 358021a2-235b-825b-e063-6394a90a76f5 | 2025-12-15 | M020 | |
| Superscreen Daytime Mineral Sunscreen | ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 35805e66-18e6-0e45-e063-6294a90afe58 | 2025-12-15 | M020 | |
| Ultra Zinc Physical Defense | ZINC OXIDE | ATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER | 35474ac4-8a9d-6a84-e063-6394a90a9bad | 2025-12-15 | M020 | |
| Ultra Zinc Physical Defense | ZINC OXIDE | ATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER | 357e315e-8802-ad73-e063-6394a90a2495 | 2025-12-15 | M020 | |
| Tinted Physical Defense | TITANIUM DIOXIDE, ZINC OXIDE | ATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER | 35477ed2-0875-58d5-e063-6294a90a3d5d | 2025-12-15 | M020 | |
| Anti Aging Daily Protection | ZINC OXIDE | LEVERRIER, KAMILA | 35465f21-8bcd-6e44-e063-6294a90a8e5f | 2025-12-15 | M020 | |
| Anti Aging Daily Protection | ZINC OXIDE | LEVERRIER, KAMILA | 3546d369-3435-b56a-e063-6294a90a0843 | 2025-12-15 | M020 | |
| Tinted Facial Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35a97770-2db9-99aa-e063-6294a90a459a | 2025-12-15 | M020 | |
| Tinted Replenishing Daily Protection | ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35a9d07d-70e5-5eed-e063-6394a90aebaf | 2025-12-15 | M020 | |
| Non-Tinted Sports Stick | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35aa833a-19a1-99e9-e063-6394a90a840f | 2025-12-15 | M020 | |
| Tinted Facial Primer | TITANIUM DIOXIDE, ZINC OXIDE | BEE NATURALS | 36c3352e-fa51-19ad-e063-6394a90a591b | 2025-12-15 | M020 | |
| Luminous Tinted Moisturizing | ZINC OXIDE | SKIN BOSS L.L.C. | 35a8ae26-82eb-e4ca-e063-6394a90a0022 | 2025-12-15 | M020 | |
| Restore Tinted Moisturizing | ZINC OXIDE | SKIN BOSS L.L.C. | 35a8e92e-ced2-fdcd-e063-6294a90acedc | 2025-12-15 | M020 | |
| Velvet Tinted Moisturizing Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN BOSS L.L.C. | 35a871dc-a707-9963-e063-6294a90a4396 | 2025-12-15 | M020 | |
| Velvet NT Moisturizing Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN BOSS L.L.C. | 35a8508d-7069-c2d6-e063-6394a90a6219 | 2025-12-15 | M020 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 44717-080-01 | 44717008001 | 88 mL in 1 TUBE (44717-080-01) | 88 ml | 2023-02-01 | No | No | Current |