warnings
Warnings Warnings For external use only When using this product - Avoid contact with eyes - Do not apply over puncture wounds, infections or lacerations Stop using and ask a doctor if - Symptoms persist more than 7 days
EIGHT HOUR NIGHT
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
- EIGHT HOUR NIGHT
- Generic name
- DIMETHICONE
- Manufacturer
- REVLON
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b3b277f9-565a-636c-e053-2995a90a94d2
- SPL ID
- 0ec6d442-3cb3-709b-e063-6394a90a795d
- Version
- 3
- Effective date
- 2024-01-12
- Source export date
- 2026-10-27
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:05:43
| 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 | M016 | openfda.application_number | |
| brand name | EIGHT HOUR NIGHT | openfda.brand_name | |
| generic name | DIMETHICONE | openfda.generic_name | |
| manufacturer name | REVLON | openfda.manufacturer_name | |
| ndc | package | 10967-675-16 | openfda.package_ndc |
| ndc | product | 10967-675 | openfda.product_ndc |
| ndc11 | package | 10967067516 | derived:openfda.package_ndc |
| spl id | 0ec6d442-3cb3-709b-e063-6394a90a795d | id | |
| spl set id | b3b277f9-565a-636c-e053-2995a90a94d2 | set_id | |
| unii | 92RU3N3Y1O | 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.