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United States · US · US:67414-226_0975230a-8706-cc07-e063-6294a90a3873
Benadryl Allergy Ultratab
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerJones Healthcare Group - Packaging Services, Inc
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1167414226002500 POUCH in 1 BOX (67414-226-00) / 2 TABLET, FILM COATED in 1 POUCH
- ndc11674142265460 POUCH in 1 CARTON (67414-226-54) / 2 TABLET, FILM COATED 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": {
"8d59d121-62a8-c43b-e053-2a95a90a5847": {
"match": "brand_token",
"title": "BENADRYL ALLERGY ULTRATAB (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [SAVINGS DISTRIBUTORS LLC]",
"spl_version": "3",
"published_date": "2026-05-13"
}
},
"productid": "67414-226_0975230a-8706-cc07-e063-6294a90a3873",
"productndc": "67414-226",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"proprietary_name": "Benadryl Allergy Ultratab",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"start_marketing_date": "20180124",
"active_numerator_strength": "25"
}Related drugs
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