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United States · US · US:73088-302_29e4f451-a6c4-c708-e063-6294a90a4649
All Over
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTubby Todd
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 8
- ndc11730883020257 g in 1 TUBE (73088-302-02)
- ndc11730883020328 g in 1 JAR (73088-302-03)
- ndc1173088302055 g in 1 PACKET (73088-302-05)
- ndc117308830208227 g in 1 JAR (73088-302-08)
- ndc11730883021010 g in 1 PACKET (73088-302-10)
- ndc11730883021515 g in 1 TUBE (73088-302-15)
- ndc117308830218227 g in 1 TUBE (73088-302-18)
- ndc11730883023599 g in 1 JAR (73088-302-35)
Annotations
UNII (FDA Substance ID)
8PI54V663Y
OATMEAL
RxCUI 221082
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "8PI54V663Y",
"rxcui": "221082",
"inchikey": null,
"display_name": "OATMEAL",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"8889af37-8345-4358-994d-7d8b847f4874": {
"match": "brand_token",
"title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
"spl_version": "6",
"published_date": "2026-05-13"
}
},
"productid": "73088-302_29e4f451-a6c4-c708-e063-6294a90a4649",
"productndc": "73088-302",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OATMEAL",
"proprietary_name": "All Over",
"active_ingred_unit": "g/100g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Colloidal Oatmeal",
"start_marketing_date": "20210420",
"active_numerator_strength": "1"
}Access this data programmatically
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