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United States · US · US:72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d
MyDerm Bite Relief
UNIISPLATC D04AB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerInspec Solutions LLC.
CountryUS (United States)
ATC codeD04AB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11726670190150 g in 1 TUBE (72667-019-01)
Annotations
UNII (FDA Substance ID)
U3RSY48JW5
BENZOCAINE
RxCUI 1399
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "U3RSY48JW5",
"rxcui": "1399",
"inchikey": "BLFLLBZGZJTVJG-UHFFFAOYSA-N",
"display_name": "BENZOCAINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"d427d623-c2fd-7d6b-e053-2995a90abdc3": {
"match": "brand_token",
"title": "MYDERM COOLING MENTHOL PAIN RELIEF WITH 50 PERCENT MORE MENTHOL (MENTHOL) GEL [INSPEC SOLUTIONS LLC.]",
"spl_version": "13",
"published_date": "2026-05-29"
}
},
"productid": "72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d",
"productndc": "72667-019",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZOCAINE",
"proprietary_name": "MyDerm Bite Relief",
"active_ingred_unit": "g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzocaine",
"start_marketing_date": "20211214",
"active_numerator_strength": "5"
}Related drugs
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