Riversol Daily Glow Mineral Tinted

Product NDC
72019-2035
11-digit product format
720192035
Labeler code
72019
Product ID
72019-2035_43cdd794-c90e-02ae-e063-6394a90a4c72
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Riversol Skincare
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-05-31
Substance
ZINC OXIDE
Active strength
132 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
SOI2LOH54ZZINC OXIDE1314-13-2ZINC OXIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72019-2035-2720192035021 BOTTLE in 1 CARTON (72019-2035-2) / 50 mL in 1 BOTTLE (72019-2035-1) 1 bottle2025-05-31NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Riversol Daily Glow Mineral TintedRiversol Skincare2025-11-17HUMAN OTC DRUG LABEL2