SEAWEED BATH CO. SPF-30

Product NDC
81159-133
11-digit product format
811590133
Labeler code
81159
Product ID
81159-133_09e272c0-a7c7-0c1f-e063-6394a90ac62e
Type
HUMAN OTC DRUG
Nonproprietary name
OCTOCRYLENE, ZINC OXIDE, OCTISALATE
Dosage form
CREAM
Route
TOPICAL
Labeler
The Seaweed Bath Co.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-11-23
Substance
OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
50; 50; 50 mg/mL; mg/mL; mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4X49Y0596WOCTISALATE118-60-5OCTISALATE
5A68WGF6WMOCTOCRYLENE6197-30-4OCTOCRYLENE
SOI2LOH54ZZINC OXIDE1314-13-2ZINC OXIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81159-133-0081159013300100 mL in 1 TUBE (81159-133-00) 100 ml2020-11-23NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SEAWEED BATH CO. SPF-30 CreamThe Seaweed Bath Co.2023-11-11HUMAN OTC DRUG LABEL2