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United States Β· US Β· US:69949-025_1461504e-866d-44d4-a4d9-60b2ba8ce33e
Mineral Sun Drops
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSynchronicity Spa, Inc. DBA Suntegrity
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1169949025011 BOTTLE, DROPPER in 1 BOX (69949-025-01) / 30 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
SOI2LOH54Z
ZINC OXIDE
RxCUI 11423
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SOI2LOH54Z",
"rxcui": "11423",
"inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
"display_name": "ZINC OXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"52462e7e-0c2c-6b64-e063-6394a90a4230": {
"match": "brand_token",
"title": "MINERAL SPF 30 MOISTURIZER CREAM [DON’T RUN OUT INC (DBA: PUBLIC GOODS)]",
"spl_version": "2",
"published_date": "2026-05-25"
}
},
"productid": "69949-025_1461504e-866d-44d4-a4d9-60b2ba8ce33e",
"productndc": "69949-025",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Mineral Sun Drops",
"active_ingred_unit": "mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide",
"start_marketing_date": "20250815",
"active_numerator_strength": "220"
}Access this data programmatically
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