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United States · US · US:85819-771_37938cce-264a-b486-e063-6394a90a17b4
SENSITIVE POCKET SUN
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerShantou Oushiya Biotechnology Co., Ltd
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1185819771435 BOTTLE, UNIT-DOSE in 1 BOX (85819-771-43) / 1 STICK in 1 BOTTLE, UNIT-DOSE
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "PERCUTANEOUS",
"spl_meta": {
"1e5e8b24-8304-482c-ae80-73effcc345da": {
"match": "brand_token",
"title": "SENSITIVE MINT TOOTH-PASTE (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [MEIJER, INC.]",
"spl_version": "4",
"published_date": "2025-12-26"
}
},
"productid": "85819-771_37938cce-264a-b486-e063-6394a90a17b4",
"productndc": "85819-771",
"dosage_form": "STICK",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CYCLOPENTASILOXANE; TALC",
"proprietary_name": "SENSITIVE POCKET SUN",
"active_ingred_unit": "mg/1; mg/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "SENSITIVE POCKET SUN",
"start_marketing_date": "20250715",
"active_numerator_strength": "26.5; 15"
}Access this data programmatically
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