warnings
WARNING FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER. DISCONTINUE USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS.
CONTROL CORRECTIVE SUNSCREEN SPF-30
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- CONTROL CORRECTIVE SUNSCREEN SPF-30
- Generic name
- OCTINOXATE, OCTISALATE, ZINC OXIDE
- Manufacturer
- CONTROL CORRECTIVE SKINCARE INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e389b2bc-bb1c-443a-9bf6-c6d96380f378
- SPL ID
- 474c0af1-db90-a31e-e063-6394a90af093
- Version
- 9
- Effective date
- 2025-12-31
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:07
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M020 | openfda.application_number | |
| brand name | CONTROL CORRECTIVE SUNSCREEN SPF-30 | openfda.brand_name | |
| generic name | OCTINOXATE, OCTISALATE, ZINC OXIDE | openfda.generic_name | |
| manufacturer name | CONTROL CORRECTIVE SKINCARE INC | openfda.manufacturer_name | |
| ndc | package | 70764-204-52 | openfda.package_ndc |
| ndc | package | 70764-204-21 | openfda.package_ndc |
| ndc | product | 70764-204 | openfda.product_ndc |
| ndc11 | package | 70764020421 | derived:openfda.package_ndc |
| ndc11 | package | 70764020452 | derived:openfda.package_ndc |
| spl id | 474c0af1-db90-a31e-e063-6394a90af093 | id | |
| spl set id | e389b2bc-bb1c-443a-9bf6-c6d96380f378 | set_id | |
| unii | SOI2LOH54Z | openfda.unii | |
| unii | 4X49Y0596W | openfda.unii | |
| unii | 4Y5P7MUD51 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.