NDC 73122-070 - RVR90 Retexturize
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
- 73122-070
- Package NDCs from labels
- 73122-070-01
- Manufacturer
- Ultraceuticals US, LLC
- Effective date
- 2023-02-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RVR90 Retexturize - Ultraceuticals US, LLC | Ultraceuticals US, LLC | 2023-02-23 | HUMAN OTC DRUG LABEL |
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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| Good Molecules Acne Foaming Cleanser | SALICYLIC ACID | Good Molecules, LLC | 44fa9eda-0910-7d70-e063-6394a90af3a7 | 2026-07-20 | Warnings | O414PZ4LPZ |
| Good Molecules Acne Foaming Cleanser | SALICYLIC ACID | Good Molecules | dec189a2-5f93-7c3e-e053-2a95a90af988 | 2026-07-20 | Warnings | O414PZ4LPZ |
| Calamine | CALAMINE AND ZINC OXIDE | Marie's Original Formulas LLC | 571083ce-cd35-a638-e063-6394a90ae4c7 | 2026-07-20 | Warnings | SOI2LOH54Z |
| Native Mineral Suncare Broad Spectrum SPF 30 Coconut and Pineapple | ZINC OXIDE | The Procter & Gamble Manufacturing Company | 3a87ddee-241d-f972-e063-6294a90a7e89 | 2026-07-20 | Warnings | SOI2LOH54Z |
| Native Mineral Suncare Daily Face Broad Spectrum SPF 30 Unscented | ZINC OXIDE | The Procter & Gamble Manufacturing Company | 3a893b13-e7f5-c5b1-e063-6394a90a4253 | 2026-07-20 | Warnings | SOI2LOH54Z |
| Omnilux Mineral Facial Sunscreen | ZINC OXIDE | The Lotus Global Group, Inc, dba GlobalMed Technologies | 5710c84b-9d6b-da4d-e063-6394a90a0737 | 2026-07-20 | Warnings | SOI2LOH54Z |
| Komxsum WART REMOVER PATCHES | SALICYLIC ACID 1% WART REMOVER | Jiangxi Yudexi Pharmaceutical Co., LTD | 4dc1da6f-661b-ae95-e063-6394a90aa414 | 2026-07-20 | Warnings | O414PZ4LPZ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.