warnings
Warnings For external use only
Vichy Laboratoires Normaderm BHA Exfoliating Serum Acne Treatment
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
- Vichy Laboratoires Normaderm BHA Exfoliating Serum Acne Treatment
- Generic name
- SALICYLIC ACID
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c6f5e9a4-c938-4c44-ace7-a9688b227d59
- SPL ID
- fb44a812-c218-45ff-b558-3db22610be6d
- Version
- 3
- Effective date
- 2023-12-11
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:39:19
| 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 | M006 | openfda.application_number | |
| brand name | Vichy Laboratoires Normaderm BHA Exfoliating Serum Acne Treatment | openfda.brand_name | |
| generic name | SALICYLIC ACID | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-230-03 | openfda.package_ndc |
| ndc | package | 49967-230-01 | openfda.package_ndc |
| ndc | package | 49967-230-02 | openfda.package_ndc |
| ndc | product | 49967-230 | openfda.product_ndc |
| ndc11 | package | 49967023003 | derived:openfda.package_ndc |
| ndc11 | package | 49967023001 | derived:openfda.package_ndc |
| ndc11 | package | 49967023002 | derived:openfda.package_ndc |
| rxcui | 245199 | openfda.rxcui | |
| spl id | fb44a812-c218-45ff-b558-3db22610be6d | id | |
| spl set id | c6f5e9a4-c938-4c44-ace7-a9688b227d59 | set_id | |
| unii | O414PZ4LPZ | 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.