SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM
- Product NDC
- 58411-296
- 11-digit product format
- 584110296
- Labeler code
- 58411
- Product ID
- 58411-296_47aab51b-96c9-d1c1-e063-6294a90a738e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE and TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- SHISEIDO AMERICAS CORPORATION
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-02-01
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 138; 123 mg/4mL; mg/4mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | I | Inactivated by FDA | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 58411-296-10 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 58411-296-10 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 58411-296-10 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 58411-296-10 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
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
- SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM
- Brand name suffix
- NATURAL LIGHT
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 138 mg/4mL |
| TITANIUM DIOXIDE | 123 mg/4mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4Y5P7MUD51 | Internal UNII lookup |
| 15FIX9V2JP | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| bf736c5b-fc33-4cd5-8d18-03929f739d76 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d1c9d1af-bddd-448d-86f7-69052b7d5b47 | Product name | 1 | 20220627 |
| 5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1 | Product name | 1 | 20201123 |
| 85bed648-23ca-4804-98e6-e36aee999cad | Product name | 1 | 20190717 |
| 80de93b4-8a94-428d-beb7-d644353ee70b | Product name | 1 | 20180424 |
| eb4f7d5b-1286-40dc-b8bf-ad87ff51c688 | Product name | 1 | 20170522 |
| db8eb201-78c7-4590-8a71-fac0a539bd8c | Product name | 1 | 20170404 |
| 141092be-5eb5-452e-9f69-2d350aa70a87 | Product name | 1 | 20161208 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 58411-296-10 | 2026-01-06 | C162847 | 48780-1 | 9d75b9d0-6be3-f424-e053-dadaa90a57ce | SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM |
| 58411-296-10 | 2025-01-31 | C162847 | 48780-1 | 9d75b9d0-6be3-f424-e053-dadaa90a57ce | SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58411-296-10 | SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUMNATURAL LIGHT | 4 mL in 1 BOTTLE | CREAM | 4 | 4 | |
| 58411-296-10 | SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUMNATURAL LIGHT | 1 in 1 CARTON | CREAM | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 58411-296 | SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM NATURAL LIGHT (OCTINOXATE AND TITANIUM DIOXIDE) CREAM SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM NATURAL (OCTINOXATE AND TITANIUM DIOXIDE) CREAM SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM MEDIUM (OCTINOXATE AND TITANIUM DIOXIDE) CREAM [SHISEIDO AMERICAS CORPORATION] | 3 | Current NDC, Legacy NDC, 2 package rows | 20231222_bf736c5b-fc33-4cd5-8d18-03929f739d76.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 |
|---|---|---|---|---|---|---|
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 31177bbd-68b0-8b24-e063-6294a90aa8d8 | 2025-12-10 | Warnings | M020 |
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 3117e138-83a1-0931-e063-6394a90abe43 | 2025-12-10 | Warnings | M020 |
| SHADED | TITANIUM DIOXIDE, ZINC OXIDE | Potency No. 710 LLC | 31188175-a4ca-449f-e063-6394a90a3c05 | 2025-12-10 | Warnings | M020 |
| COVERED | ZINC OXIDE | Potency No. 710 LLC | 3118c3ed-f0f0-f997-e063-6294a90a53a9 | 2025-12-10 | Warnings | M020 |
| COVERED | ZINC OXIDE | Potency No. 710 LLC | 3117faeb-1792-1b2e-e063-6294a90a92df | 2025-12-10 | Warnings | M020 |
| Non-Tinted Mineral Foaming Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Restore Skin Therapy, LLC | 364b6af2-a0ed-4a17-e063-6394a90a3a17 | 2025-12-10 | M020 | |
| Morning Replenish | ZINC OXIDE | Restore Skin Therapy, LLC | 364b26c2-a1bb-9660-e063-6294a90a14d1 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Tinted | ZINC OXIDE | Fleur de Lune, LLC | 34288989-35b8-3aa3-e063-6394a90ac2c4 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Tinted | ZINC OXIDE | Fleur de Lune, LLC | 3418394b-fede-65ce-e063-6394a90ad5f9 | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Non-Tinted | ZINC OXIDE | Fleur de Lune, LLC | 341871e5-c170-7560-e063-6394a90a8eee | 2025-12-10 | M020 | |
| Glass Skin Sunscreen Non-Tinted | ZINC OXIDE | Fleur de Lune, LLC | 3428bdbb-1f18-a29b-e063-6294a90addbc | 2025-12-10 | M020 | |
| Sheer Facial Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342b2403-4f4a-3e77-e063-6294a90a4f0a | 2025-12-10 | M020 | |
| Sheer Mineral Sunscreen Bar | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342b69d5-f0e1-99cd-e063-6294a90abb6e | 2025-12-10 | M020 | |
| Sheer Facial Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | BB MEDICAL & DERMATOLOGY INC | 342c3f42-c17f-f777-e063-6394a90a8058 | 2025-12-10 | M020 | |
| Lip SPF | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396d3fdd-99d8-77e8-e063-6294a90aec2f | 2025-12-10 | M020 | |
| Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396cae82-7641-e1b2-e063-6394a90a7c07 | 2025-12-10 | M020 | |
| Solar Knight SPF 40 Broad Spectrum | TITANIUM DIOXIDE, ZINC OXIDE | MASCARENAS ENTERPRISES, INC. | 36c27c91-22ac-205c-e063-6294a90ab379 | 2025-12-10 | M020 | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | FRANCISCO FLORES, M.D., P.A. | 396ce15a-06ad-4055-e063-6294a90a27fb | 2025-12-10 | M020 | |
| Dermablue Daily Replenishing | ZINC OXIDE | Dermablue, P.C. | 308da9c9-544e-d5d1-e063-6294a90aa49b | 2025-12-10 | Warnings | M020 |
| Recoverie Mineral Matte | ZINC OXIDE | Clear Day Acne Clinic | 308f41de-fb14-40f9-e063-6394a90a008f | 2025-12-10 | Warnings | M020 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 58411-296-10 | 58411029610 | 1 BOTTLE in 1 CARTON (58411-296-10) / 4 mL in 1 BOTTLE | 1 bottle | 2017-02-01 | 0000-00-00 | No | No | Current |