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United States · US · US:57598-888_46879b8b-9d05-4457-99ad-ddd77d90ceb7
Ultra Balm
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLing Nam Medicine Factory (H.K.) Ltd.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1157598888071 JAR in 1 CARTON (57598-888-07) / 19.8 g in 1 JAR
- ndc1157598888231 JAR in 1 CARTON (57598-888-23) / 65.1 g in 1 JAR
- ndc1157598888881 JAR in 1 CARTON (57598-888-88) / 65.1 g in 1 JAR
Annotations
UNII (FDA Substance ID)
L7T10EIP3A
MENTHOL, UNSPECIFIED FORM
RxCUI 6750
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "L7T10EIP3A",
"rxcui": "6750",
"inchikey": null,
"display_name": "MENTHOL, UNSPECIFIED FORM",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"52d4b1c1-7431-4f8c-e063-6294a90ad482": {
"match": "brand_token",
"title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
"spl_version": "1",
"published_date": "2026-05-29"
}
},
"productid": "57598-888_46879b8b-9d05-4457-99ad-ddd77d90ceb7",
"productndc": "57598-888",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE",
"proprietary_name": "Ultra Balm",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Menthol and Methyl Salicylate",
"start_marketing_date": "20130801",
"active_numerator_strength": "140; 232"
}Access this data programmatically
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