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United States · US · US:82568-0008_354289e0-a1d5-590d-e063-6394a90a2ec3
Children Acetaminophen
UNIISPLATC N02BE51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAARNA USA INC.
CountryUS (United States)
ATC codeN02BE51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1182568000841 BOTTLE in 1 PACKAGE (82568-0008-4) / 118 mL in 1 BOTTLE
- ndc118256800086473 mL in 1 BOTTLE (82568-0008-6)
- ndc1182568000881 BOTTLE in 1 PACKAGE (82568-0008-8) / 236 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "362O9ITL9D",
"rxcui": "161",
"inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
"display_name": "ACETAMINOPHEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a26c3515-4a24-4988-b9bb-813420b15630": {
"match": "brand_token",
"title": "CHILDREN ALLERGY (FEXOFENADINE HCL) SUSPENSION [H E B]",
"spl_version": "3",
"published_date": "2026-05-13"
}
},
"productid": "82568-0008_354289e0-a1d5-590d-e063-6394a90a2ec3",
"productndc": "82568-0008",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN",
"proprietary_name": "Children Acetaminophen",
"active_ingred_unit": "mg/5mL",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen",
"start_marketing_date": "20250218",
"active_numerator_strength": "160"
}Related drugs
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