Principal Secret

Manufacturer
Guthy-Renker LLC
Effective date
2010-07-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:39

Label at a glance#

ProductPrincipal Secret Advanced with Hydrospheres Continuous Moisture SPF8
Active ingredientOctinoxate, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

To Use

INDICATIONS & USAGE SECTION

Apply with a gentle upward motion to face and neck.

WARNING

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, flush thoroughly with water.

OTC - STOP USE SECTION

If irritation develops, discontinue use.

OTC - DO NOT USE SECTION

Do not use on infants under 6 months old.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate (7.5%), Octisalate (1.0%)

Other Ingredients

INACTIVE INGREDIENT SECTION

Water (Eau), Ethylhexyl Palmitate, Cetyl Lactate, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Cetyl Dimethicone, Yeast Extract (Extrait de levure), Retinyl Palmitate, Tocopheryl Linoleate, Panthenol, Sodium Hyaluronate, Vitis Vinifera (Grape) Seed Extract, Phospholipids, Tocopheryl Acetate, Ascorbyl Palmitate, Pantothenic Acid, Phytonadione, Citrus Aurantium Dulcis (Orange) Oil, Limonene, Magnesium Ascorbyl Phosphate, Avena Sativa (Oat) Kernel Extract, Papain, Lecithin, Polyacrylamide, Laureth-7, C13-14 Isoparaffin, PEG-8/SMDI Copolymer, Triethanolamine, Carbomer, Trisodium EDTA, Phenoxyethanol, Methylparaben, Propylparaben

SPL UNCLASSIFIED SECTION

Distributed by Guthy-Renker
Palm Desert, CA 92260,
Guthy Renker® (UK) Ltd.,
London UK WC2E 8AA,
Sydney Australia 2138,
Auckland New Zealand,
Toronto Ontario Canada M1B 3W2

PRINCIPAL DISPLAY PANEL - 57g Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ADVANCED
WITH
HYDROSPHERES ®

Continuous Moisture ® SPF 8

PRINCIPAL DISPLAY PANEL - 57g Label
PRINCIPAL DISPLAY PANEL - 57g Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11410-541-342020-01-29C16284748780-1956f9ecf-ca3b-621f-e053-dbdaa90a74adADVANCED CONTINUOUS MOISTURE ® SPF 8
11410-541-342019-10-21C16284748780-1956f9ecf-ca3b-621f-e053-dbdaa90a74adADVANCED CONTINUOUS MOISTURE ® SPF 8

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctisalateACTIVE INGREDIENT4X49Y0596W1
OctinoxateACTIVE MOIETY4Y5P7MUD511
OctisalateACTIVE MOIETY4X49Y0596W1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11410-54111410-541-34

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Octinoxate4Y5P7MUD51ACTIB
Octisalate4X49Y0596WACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
48c30b3c-7c9c-4371-a3b4-1443d9269a4d1f923d90-3617-462c-bc4d-61a4d2f479b22010-07-19WarningsExact identifier
spl id: 48c30b3c-7c9c-4371-a3b4-1443d9269a4d
spl set id: 1f923d90-3617-462c-bc4d-61a4d2f479b2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.