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United States · US · US:11383-192_28650b5a-ed6f-199c-e063-6394a90a9dac
Bite and Itch
UNIISPLATC D04AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWeeks & Leo Co., Inc.
CountryUS (United States)
ATC codeD04AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1111383192011 BOTTLE in 1 CARTON (11383-192-01) / 118 mL in 1 BOTTLE
- ndc111138319204118 mL in 1 BOTTLE (11383-192-04)
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": "CUTANEOUS",
"spl_meta": {
"0a4d471b-c3f3-0a6a-e063-6394a90ad57b": {
"match": "brand_token",
"title": "BITE AND ITCH (DIPHENHYDRAMINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE) LOTION [WEEKS & LEO CO., INC.]",
"spl_version": "3",
"published_date": "2024-12-06"
}
},
"productid": "11383-192_28650b5a-ed6f-199c-e063-6394a90a9dac",
"productndc": "11383-192",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE",
"proprietary_name": "Bite and Itch",
"active_ingred_unit": "g/100mL; g/100mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Diphenhydramine Hydrochloride, Pramoxine Hydrochloride",
"start_marketing_date": "20150615",
"active_numerator_strength": "2; 1"
}Related drugs
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