warnings
■ For external use only. ■ Do not use in eyes. ■ lf swallowed, get medical help promptly. ■ Stop use, ask doctor lf irritation occurs. ■ Keep out of reach of children.
DEFENDER SIGNATURE
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
- DEFENDER SIGNATURE
- Generic name
- SODIUM CHLORITE
- Manufacturer
- Pure O2
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c029345a-d44b-74db-e053-2995a90a1dbe
- SPL ID
- c0293cb2-be63-25bb-e053-2995a90a9d6a
- Version
- 1
- Effective date
- 2021-04-17
- Source export date
- 2026-10-27
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:47:36
| 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 |
|---|---|---|---|
| brand name | DEFENDER SIGNATURE | openfda.brand_name | |
| generic name | SODIUM CHLORITE | openfda.generic_name | |
| manufacturer name | Pure O2 | openfda.manufacturer_name | |
| ndc | package | 75124-0012-1 | openfda.package_ndc |
| ndc | product | 75124-0012 | openfda.product_ndc |
| ndc11 | package | 75124001201 | derived:openfda.package_ndc |
| spl id | c0293cb2-be63-25bb-e053-2995a90a9d6a | id | |
| spl set id | c029345a-d44b-74db-e053-2995a90a1dbe | set_id | |
| unii | G538EBV4VF | 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.