warnings
Warnings For external use only. If skin condition persists after 7 days, or returns, consult a physician immediately. If pregnant or breastfeeding, as a health professional before use.
emuaidMAX Concentrate
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
- emuaidMAX Concentrate
- Generic name
- SILVER
- Manufacturer
- Speer Laboratories, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1fe32c32-1694-4df6-aacc-3a70f4383b95
- SPL ID
- 9d31bf43-415d-410a-8c41-a641b9698849
- Version
- 1
- Effective date
- 2023-11-13
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:38:49
| 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 | emuaidMAX Concentrate | openfda.brand_name | |
| generic name | SILVER | openfda.generic_name | |
| manufacturer name | Speer Laboratories, LLC | openfda.manufacturer_name | |
| ndc | package | 55926-0027-2 | openfda.package_ndc |
| ndc | product | 55926-0027 | openfda.product_ndc |
| ndc11 | package | 55926002702 | derived:openfda.package_ndc |
| spl id | 9d31bf43-415d-410a-8c41-a641b9698849 | id | |
| spl set id | 1fe32c32-1694-4df6-aacc-3a70f4383b95 | set_id | |
| unii | 3M4G523W1G | 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.