FDA.reportPublic FDA data

CONSCIOUS SUNSCREEN, PROTECT-RESPECT, FACE

Manufacturer
SOLID SKIN LLC | HealthSpecialty
Effective date
2020-01-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:45:24

Label at a glance#

ProductCONSCIOUS SUNSCREEN, PROTECT-RESPECT, FACE SPF-40
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

HELPS PREVENT SUNBURN. IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER, EARLY SKIN AGING BY THE SUN.

Dosage and administration

APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE. REAPPLY: AFTER 80 MINUTES OF SWIMMING OR SWEATING AT LEAST EVERY 2 HOURS OR IMMEDIATELY AFTER TOWEL DRYING. SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THE RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING: LIMIT TIME IN THE S...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

MICRONIZED ZINC OXIDE  17%

TITANIUM DIOXIDE  3%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

HELPS PREVENT SUNBURN. IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER, EARLY SKIN AGING BY THE SUN.

WARNING

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.
  • DO NOT USE ON DAMAGED OR BROKEN SKIN.
  • STOP USE AND CONTACT A DOCTOR IS RASH OCCURS.
  • WHEN USING THIS PRODUCT KEEP  OUT OF EYES. RINSE WITH WATER TO REMOVE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • KEEP OUT OF REACH OF CHILDREN.
  • IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.

REAPPLY:

  • AFTER 80 MINUTES OF SWIMMING OR SWEATING
  • AT LEAST EVERY 2 HOURS OR IMMEDIATELY AFTER TOWEL DRYING.

SUN PROTECTION MEASURES:

SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY SKIN AGING. TO DECREASE THE RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:

  • LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 AM - 2 PM
  • WEAR LONG-SLEEVE SHIRTS, PANTS, HATS AND SUNGLASSES
  • CHILDREN UNDER 6 MONTHS, ASK A DOCTOR

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

CASTOR SEED OIL, BEESWAX, C12-15 ALKYL BENZOATE, CAPRYLIC CAPRIC TRIGLYCERIDES, DICAPRYLYL ETHER, CARNAUBA WAX, SHEA BUTTER, KAOLIN, VITAMIN E ACETATE, ALOE LEAF JUICE, GREEN TEA EXTRACT, SEA KELP EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

solid_FaceStick_4.10solid_FaceStick_4.10

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71524-102-112024-04-01C16284748780-1d6a99b39-6c7a-a426-e053-dadaa90af4c262b296f8-6572-4f1d-9232-4e809e071f1b
71524-102-112022-01-28C16284748780-1d6a99b39-6c7a-a426-e053-dadaa90af4c262b296f8-6572-4f1d-9232-4e809e071f1b

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71524-10271524-102-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIM
TITANIUM DIOXIDE15FIX9V2JPACTIB
CASTOR OILD5340Y2I9GIACT
YELLOW WAX2ZA36H0S2VIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
DICAPRYLYL ETHER77JZM5516ZIACT
CARNAUBA WAXR12CBM0EIZIACT
SHEA BUTTERK49155WL9YIACT
KAOLIN24H4NWX5COIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
MACROCYSTIS PYRIFERAK31S3OG5C4IACT

Source Document#

Source XML · Source PDF

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
150fb675-6d8e-0e74-e063-6394a90a482662b296f8-6572-4f1d-9232-4e809e071f1b2024-04-01WarningsExact identifier
spl set id: 62b296f8-6572-4f1d-9232-4e809e071f1b

Reported adverse events (FAERS/openFDA)#

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