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United States · US · US:82706-021_1cd2a6f1-31ae-e507-e063-6394a90aba58
AXIV Allergy Relief
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerVIVUNT PHARMA LLC
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11827060210250 POUCH in 1 CARTON (82706-021-02) / 2 TABLET in 1 POUCH
Annotations
UNII (FDA Substance ID)
TC2D6JAD40
DIPHENHYDRAMINE HYDROCHLORIDE
RxCUI 1362
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "TC2D6JAD40",
"rxcui": "1362",
"inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
"display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4b81abf9-3ea7-e996-e063-6394a90a71e8": {
"match": "brand_token",
"title": "AXIV SINUS SEVERE ULTRA FINE MIST (OXYMETAZOLINE HYDROCHLORIDE.) AEROSOL, SPRAY [VIVUNT PHARMA LLC]",
"spl_version": "2",
"published_date": "2026-04-13"
}
},
"productid": "82706-021_1cd2a6f1-31ae-e507-e063-6394a90aba58",
"productndc": "82706-021",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"proprietary_name": "AXIV Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Diphenhydramine Hydrochloride",
"start_marketing_date": "20240709",
"active_numerator_strength": "25"
}Related drugs
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