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United States · US · US:67777-555_45878c3c-d05e-984c-e063-6294a90a4661
AquaSoothe
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDynarex Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11677775550224 TUBE in 1 CASE (67777-555-02) / 106 g in 1 TUBE (67777-555-01)
- ndc11677775550412 JAR in 1 CASE (67777-555-04) / 396.9 g in 1 JAR (67777-555-03)
- ndc11677775550612 BOX in 1 CASE (67777-555-06) / 144 PACKET in 1 BOX (67777-555-05) / .9 g in 1 PACKET
Annotations
UNII (FDA Substance ID)
4T6H12BN9U
PETROLATUM
RxCUI 8091
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4T6H12BN9U",
"rxcui": "8091",
"inchikey": null,
"display_name": "PETROLATUM",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"45878c3c-d05d-984c-e063-6294a90a4661": {
"match": "brand_token",
"title": "AQUASOOTHE OINTMENT [DYNAREX CORPORATION]",
"spl_version": "1",
"published_date": "2025-12-16"
}
},
"productid": "67777-555_45878c3c-d05e-984c-e063-6294a90a4661",
"productndc": "67777-555",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PETROLATUM",
"proprietary_name": "AquaSoothe",
"active_ingred_unit": "g/100g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "AquaSoothe",
"start_marketing_date": "20251216",
"active_numerator_strength": "41"
}Access this data programmatically
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