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United States · US · US:67676-101_08b4632c-2421-6046-e063-6294a90a1527
OsmoFlex
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSarati International, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116767610101113.4 g in 1 TUBE (67676-101-01)
- ndc116767610103964.3 g in 1 BOTTLE (67676-101-03)
- ndc116767610104453.6 g in 1 BOTTLE (67676-101-04)
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "TOPICAL",
"spl_meta": {
"479147c0-4cf4-4d7a-8b8e-1a0de49ed73e": {
"match": "brand_token",
"title": "OSMOFLEX (MENTHOL) CREAM [SARATI INTERNATIONAL, INC.]",
"spl_version": "7",
"published_date": "2023-11-02"
}
},
"productid": "67676-101_08b4632c-2421-6046-e063-6294a90a1527",
"productndc": "67676-101",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MENTHOL",
"proprietary_name": "OsmoFlex",
"active_ingred_unit": "g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "MENTHOL",
"start_marketing_date": "20160516",
"active_numerator_strength": "1.3"
}Access this data programmatically
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