NATURAL MINERAL BODY SUNSCREEN

Product NDC
69949-100
11-digit product format
699490100
Labeler code
69949
Product ID
69949-100_63ef5062-4f1d-4f7a-b1a2-88814db88ca3
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
69949-100-016994901000185 g in 1 TUBE (69949-100-01) 85 g2010-08-12NoNoHistorical
69949-100-0269949010002141.7 g in 1 TUBE (69949-100-02) 141.7 g2010-08-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NATURAL MINERAL BODY SUNSCREENSynchronicity Spa, Inc. DBA Suntegrity2024-11-21HUMAN OTC DRUG LABEL2