warnings
Warnings Stop use and ask a doctor if ■ symptoms persist for more than 72 hours or worsen. ■ symptoms are accompanied by a fever. If pregnant or breastfeeding ask a health professional before use. Keep out of reach of children.
4 Kids Stuffy Nose and Sinus
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
- 4 Kids Stuffy Nose and Sinus
- Generic name
- PULSATILLA PRATENSIS WHOLE,OYSTER SHELL CALCIUM CARBONATE, CRUDE,GOLDENSEAL AND POTASSIUM DICHROMATE
- Manufacturer
- Hylands Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a00f1db3-cae4-5729-e053-2a95a90ab001
- SPL ID
- 387c5392-b956-044f-e063-6394a90a9d86
- Version
- 6
- Effective date
- 2025-06-26
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:13
| Harmonized routes |
|---|
| ORAL |
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 | 4 Kids Stuffy Nose and Sinus | openfda.brand_name | |
| generic name | PULSATILLA PRATENSIS WHOLE,OYSTER SHELL CALCIUM CARBONATE, CRUDE,GOLDENSEAL AND POTASSIUM DICHROMATE | openfda.generic_name | |
| manufacturer name | Hylands Inc. | openfda.manufacturer_name | |
| ndc | package | 54973-3406-2 | openfda.package_ndc |
| ndc | package | 54973-3406-1 | openfda.package_ndc |
| ndc | product | 54973-3406 | openfda.product_ndc |
| ndc11 | package | 54973340601 | derived:openfda.package_ndc |
| ndc11 | package | 54973340602 | derived:openfda.package_ndc |
| spl id | 387c5392-b956-044f-e063-6394a90a9d86 | id | |
| spl set id | a00f1db3-cae4-5729-e053-2a95a90ab001 | set_id | |
| unii | 2E32821G6I | openfda.unii | |
| unii | 8E272251DI | openfda.unii | |
| unii | ZW3Z11D0JV | openfda.unii | |
| unii | T4423S18FM | 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.