warnings
do not use for the following people: infants under six months do not use excessive amounts or for long periods of time beyond the required do not use it in an enclosed area
MOSQUITO BUG OFF
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
- MOSQUITO BUG OFF
- Generic name
- DIETHYLTOLUAMIDE
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 84caf0f9-19e5-4079-e053-2a91aa0a8969
- SPL ID
- c5cd92d6-2be7-73c6-e053-2995a90a3ea3
- Version
- 6
- Effective date
- 2021-06-28
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:59:53
| 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 | MOSQUITO BUG OFF | openfda.brand_name | |
| generic name | DIETHYLTOLUAMIDE | openfda.generic_name | |
| manufacturer name | Lydia Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 72988-0005-1 | openfda.package_ndc |
| ndc | product | 72988-0005 | openfda.product_ndc |
| ndc11 | package | 72988000501 | derived:openfda.package_ndc |
| spl id | c5cd92d6-2be7-73c6-e053-2995a90a3ea3 | id | |
| spl set id | 84caf0f9-19e5-4079-e053-2a91aa0a8969 | set_id | |
| unii | FB0C1XZV4Y | 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.