SUN DMC

Manufacturer
LET IT BLOCK LLC
Effective date
2016-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:27:35

Label at a glance#

ProductSUN DMC SPF-30
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 SUN CANCER, EARLY AGEING BY THE SUN.   

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE 5 %

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 SUN CANCER, EARLY AGEING BY THE SUN.   

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

DO NOT USE ON DAMAGED OR BROKEN SKIN.

WHEN USINGT THIS PRODUCT KEEP OUT OF EYES.  RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURES.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REWACH OF YOUNG CHILDREN.  IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR

CONTACT A POISION CONTROL CENTER RIGHT AWAY.   

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.

REAPPLY:  AFTER 80 MINUTES OF SWIMMINGF OR SWEATING

                 AT LEAST EVERY 2 HOURS. IMMEDIATELY AFTER TOWEL DRYING.

SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY

SKIN AGEING. TO DECREASE THIS RISK, REGULALY USE OF A SUNSCREEN WITH BROAD SPECTRUM SPF OF

15 OR HIGHER AND OTHER DUN PROTECTION INCLUDING:

  LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 A.M. - 2 P.M.

  WEAR LONG SLEEVE SHIRTS, PANTS, HATS AND SUNGLASSES

CHILDREN UNDER 6 MONTHS.  ASK A DOCTOR.   

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water, Caprylic Capric Triglycerides, Ethylhexyl Palmitate, C12-C15 Alkyl, Benzoate, Isopropyl Palmitate, Glycerin, Cetearyl Alcohol (and) Cetearyl Glucoside, Acrylates/C12-22 Alkylmethacrylate Copolymer, Acrylates Copolymer, Glyceryl Stearate (and) Peg-10 Stearate, Sodium HydroxymethylglycinateXanthan Gum, Aloe Barbadensis Leaf Juice, Isostearic Acid, Polyhydroxystearic Acid, Sodium Ascorbyl Phosphate, Green Tea Extract, Helianthus Annuus (Sunflower) Seed Oil, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Punica Granatum Extract, Vaccinium Angustifolium (Blueberry) Extract, Fragaria Vesca (Strawberry) Fruit Extract Actinidia, Chinensis (Kiwi) Extract, Citrullus Vulgaris (Watermelon) Fruit Extract, Vitis Vinifera (Grape) Seed Extract, Rubus Idaeus Seed Extract, Myrciaria dubia (Camu Camu) Fruit Extract,Euterpe Oleracea Fruit Extract, Lycium Barbarum (Goji) Extract, Hippophae Rhamnoides (Sea Buckthorn) Fruit Extract, Cannabis Sativa (Hemp) Seed Extract, Brassica Oleracea Italica(Broccoli) Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUN DMC PACKAGE ARTSUN DMC PACKAGE ART

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70640-101-132024-04-01C16284748780-19d75b9d0-cf07-f424-e053-dadaa90a57cefb379d72-4792-4d0a-9a4d-d82d65baf15c
70640-101-132020-01-31C16284748780-19d75b9d0-cf07-f424-e053-dadaa90a57cefb379d72-4792-4d0a-9a4d-d82d65baf15c

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70640-10170640-101-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

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
150f305c-e83d-34c3-e063-6294a90aa51afb379d72-4792-4d0a-9a4d-d82d65baf15c2024-04-01WarningsExact identifier
spl set id: fb379d72-4792-4d0a-9a4d-d82d65baf15c

Reported adverse events (FAERS/openFDA)#

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