NU-DERM HEALTHY SKIN PROTECTION
- Product NDC
- 62032-200
- 11-digit product format
- 620320200
- Labeler code
- 62032
- Product ID
- 62032-200_c8e9655e-6ce4-4a41-a31d-896bfde6f0af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE and ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Obagi Cosmeceuticals LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2002-01-01
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 75; 90 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 62032-200 | 62032-200-90 | D | Discontinued by firm | 2026-10-05 |
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 package | package | 62032-200-90 | D | Discontinued by firm | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 62032-200-90 | D | Discontinued by firm | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 62032-200-90 | D | Discontinued by firm | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 62032-200-90 | D | Discontinued by firm | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 62032-200-90 | D | Discontinued by firm | 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 | 62032-200-90 | D | Discontinued by firm | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 62032-200-01 | 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 | 62032-200-90 | D | Discontinued by firm | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 62032-200-01 | 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 | 62032-200-90 | D | Discontinued by firm | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 62032-200-01 | 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 | 62032-200-90 | D | Discontinued by firm | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 62032-200-01 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 62032-200-90 | D | Discontinued by firm | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 62032-200-90 | D | Discontinued by firm | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded package | package | 62032-200-90 | D | Discontinued by firm | 557ba5c1ecfa… | 9c80585c8c6e… |
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
- NU-DERM HEALTHY SKIN PROTECTION
- Brand name suffix
- SPF 35
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OCTINOXATE | 75 mg/mL |
| ZINC OXIDE | 90 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4Y5P7MUD51 | Internal UNII lookup |
| SOI2LOH54Z | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| cfb6a918-1403-4cf2-86d8-d66dd764bb6c | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 597b1cfd-7b31-5048-62be-ca5cd740da2f | Product name | 1 | 20140508 |
| 85490a6b-2306-6bf2-c51b-eb63537dc2da | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 62032-200-01 | 2025-03-14 | NU-DERM HEALTHY SKIN PROTECTION SPF 35 |
| 62032-200-90 | 2025-03-14 | NU-DERM HEALTHY SKIN PROTECTION SPF 35 |
| 62032-200-01 | 2025-01-30 | NU-DERM HEALTHY SKIN PROTECTION SPF 35 |
| 62032-200-90 | 2025-01-30 | NU-DERM HEALTHY SKIN PROTECTION SPF 35 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62032-200-01 | NU-DERM HEALTHY SKIN PROTECTIONSPF 35 | 1 in 1 CARTON | CREAM | 1 | 7 | |
| 62032-200-01 | NU-DERM HEALTHY SKIN PROTECTIONSPF 35 | 85 mL in 1 BOTTLE, PLASTIC | CREAM | 85 | 7 | |
| 62032-200-90 | NU-DERM HEALTHY SKIN PROTECTIONSPF 35 | 90 mL in 1 BOTTLE, PLASTIC | CREAM | 90 | 7 | |
| 62032-200-10 | NU-DERM STARTER SET NORMAL-DRYSKIN TRANSFORMATION SYSTEM | 30 mL in 1 BOTTLE, PLASTIC | CREAM | 30 mL | 90 mg in 1mL | 1 |
| 62032-200-10 | NU-DERM STARTER SET NORMAL-OILYSKIN TRANSFORMATION SYSTEM | 30 mL in 1 BOTTLE, PLASTIC | CREAM | 30 mL | 90 mg in 1mL | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 62032-200 | NU-DERM HEALTHY SKIN PROTECTION SPF 35 (OCTINOXATE AND ZINC OXIDE) CREAM [OBAGI COSMECEUTICALS LLC] | 7 | Current NDC, Legacy NDC, 3 package rows | 20250316_cfb6a918-1403-4cf2-86d8-d66dd764bb6c.zip |
| 62032-200 | NU-DERM STARTER SET NORMAL-DRY SKIN TRANSFORMATION SYSTEM ( HYDROQUINONE, OCTINOXATE, OXYBENZONE AND ZINC OXIDE) KIT [OMP, INC.] | 1 | Current NDC, Legacy NDC | 20120521_f439d77f-ec5b-4534-a005-08f2e7af8d0c.zip |
| 62032-200 | NU-DERM STARTER SET NORMAL-OILY SKIN TRANSFORMATION SYSTEM ( HYDROQUINONE, OCTINOXATE, OXYBENZONE AND ZINC OXIDE) KIT [OMP, INC.] | 1 | Current NDC, Legacy NDC | 20120521_c67b0629-5529-412d-99ee-186df4ecad5a.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.
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197795 | hydroquinone 4 % Topical Cream | PSN | c67b0629-5529-412d-99ee-186df4ecad5a | 1 |
| 197795 | hydroquinone 4 % Topical Cream | PSN | f439d77f-ec5b-4534-a005-08f2e7af8d0c | 1 |
| 197795 | hydroquinone 40 MG/ML Topical Cream | SCD | c67b0629-5529-412d-99ee-186df4ecad5a | 1 |
| 197795 | hydroquinone 40 MG/ML Topical Cream | SCD | f439d77f-ec5b-4534-a005-08f2e7af8d0c | 1 |
| 197795 | hydroquinone 4 % Topical Cream | SY | c67b0629-5529-412d-99ee-186df4ecad5a | 1 |
| 197795 | hydroquinone 4 % Topical Cream | SY | f439d77f-ec5b-4534-a005-08f2e7af8d0c | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 62032-200-01 | 62032020001 | 1 BOTTLE, PLASTIC in 1 CARTON (62032-200-01) / 85 mL in 1 BOTTLE, PLASTIC | 2020-04-01 | 0000-00-00 | No | No | Current | |
| 62032-200-10 | 62032020010 | 30 mL in 1 BOTTLE, PLASTIC | 30 ml | Historical | ||||
| 62032-200-90 | 62032020090 | 90 mL in 1 BOTTLE, PLASTIC | 90 ml | Historical |