NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER

Product NDC
69949-010
11-digit product format
699490010
Labeler code
69949
Product ID
69949-010_3dc666fa-dd86-4924-9b90-50d240203981
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Synchronicity Spa, Inc. DBA Suntegrity
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2010-08-12
Substance
ZINC OXIDE
Active strength
200 mg/g
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
69949-010-016994900100150 g in 1 CANISTER (69949-010-01) 50 g2010-08-12NoNoHistorical
69949-010-026994900100250 g in 1 BOX (69949-010-02) 50 g2020-07-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NATURAL MOISTURIZING FACE SUNSCREEN & PRIMERSynchronicity Spa, Inc. DBA Suntegrity2024-11-21HUMAN OTC DRUG LABEL2