NDC 83103-2575-01 - Ciele Blush and Protect Berri
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 83103-2575
- Requested NDC
- 83103-2575-01
- Package NDCs from labels
- 83103-2575-1, 83103-2575-2, 83103-2575-3, 83103-2575-01
- Manufacturer
- Ciele LLC
- Effective date
- 2026-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ciele Blush and Protect Berri - Ciele LLC | Ciele LLC | 2026-05-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83103-2575-1 | Ciele Blush and Protect Berri | 5.5 mL in 1 BOTTLE, WITH APPLICATOR | LOTION | 5.5 | 2 | |
| 83103-2575-2 | Ciele Blush and Protect Berri | 1 in 1 CARTON | LOTION | 1 | 2 | |
| 83103-2575-3 | Ciele Blush and Protect Berri | 2.7 mL in 1 BOTTLE, WITH APPLICATOR | LOTION | 2.7 | 2 |
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.
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| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 93aeac13-41de-4452-9f38-d6b4f38ada30 | 2025-01-24 | 451W47IQ8X | |
| CoTZ Silky Foam Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD | 9c04b76e-ae65-4183-b475-3b8e8764db59 | 2025-01-24 | Warnings | M020 SOI2LOH54Z 15FIX9V2JP |
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| Soleo Organics Sunscreen | ZINC OXIDE | SE Operations Pty Ltd | 59ea43e3-f6e6-4d10-9d8f-2f14eaf2f79b | 2025-01-22 | Warnings | M020 SOI2LOH54Z |
| Neptune Ave. High Dive Barrier Repair Moisturizer Broad Spectrum SPF 50 | AVOBENZONE, OCTISALATE, OCTOCRYLENE | Neptune Ave. Inc. | 25034563-6420-daf6-e063-6394a90af980 | 2025-01-22 | Warnings | M020 |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DOCSMEDI Co., Ltd. | a02f8865-e7be-4ef4-b09c-dad846639764 | 2025-01-22 | Warnings | ETJ7Z6XBU4 |
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| Jafra Royal Defy Sample Kit | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Distribuidora Comercial Jafra, S.A. de C.V. | c3b265b1-ab84-4ea9-b283-c92f5a4cf461 | 2025-01-22 | Warnings | M020 |
| SUNSCREEN BROAD SPECTRUM SPF 50 FACE AND BODY | AVOBENZONE/OCTISALATE/OCTOCRYLENE | Mary Kay Inc. | 2c4eaf2e-b034-8185-e063-6394a90a8275 | 2025-01-22 | Warnings | M020 |
| Prunus Iron | PRUNUS IRON | Uriel Pharmacy Inc. | 091be588-b62e-4919-8e9e-3edb9792d319 | 2025-01-22 | Warnings | 1K09F3G675 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.