NWC21 NATURAL SUN PROTECTOR

Manufacturer
CLEANSIA CORPORATION LTD.
Effective date
2010-09-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:25:43

Label at a glance#

ProductNWC21 NATURAL SUN PROTECTOR SPF50
Active ingredientTITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: TITANIUM DIOXIDE

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Cyclopentasiloxane, Ethylhexyl Methoxycinnamate, C12-15 Alkyl Benzoate, Ethylhexyl Salicylate, Butylene Glycol, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine,
Isoamyl p-Methoxycinnamate, Cetyl PEG/PPG-10/1 Dimethicone, Beeswax, Disteardimonium Hectorite, Glycerin, Sodium Chloride, Aluminum Stearate, Dimethicone Crosspolymer, Cetearyl Alcohol, Polyhydroxystearic Acid, Microcrystalline Wax, Phenoxyethanol, Alumina, Methylparaben, Propylparaben, Xanthan Gum, Dipotassium Glycyrrhizate, Polyglutamic Acid, Oryza Sativa (Rice) Bran Extract, Fragrance

DESCRIPTION SECTION

Directions:
When you use or do leisure, apply reasonable amount on your body exposed to UV including face, neck, arms, and legs at your finishing step of basic makeup.
Take more frequent reapplication for longtime outdoor activities.

Notice for use:
1. Discontinue if the following symptom appears and consult with dermatologist for the continuos problem of use.
  1) Discontinue use if redness, rash, irritation or tingling appears.
  2) Discontinue if the above symptom appears by a direct sunlight on the applied part.
2. Avoid the part for a cut, eczema or dermatitis.
3. Please note for keeping and handling.
  1) To keep the freshness, please close the lid after the use.
  2) Keep this and all drugs out of reach of children.
  3) Do not store this product in a place of high or low temperature. Do not expose it to the direct sunlight.
  4) Be careful, it may be slipper when contact with the product.
  5) Be careful not to make contacts with clothes.
  6) Be careful not to give a shock since the container may be broken and get injured.
  7) UV cutoff rating and SPF rating A of this product was measured in accordance with UV cutoff rating effect and methods examined by Korea Food and Drug Administration.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
45167-040-012019-10-21C16284748780-1956f9ecf-d5d8-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45167-040-01NWC21 NATURAL SUN PROTECTORSPF5060 mL in 1 CARTONCREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45167-040NWC21 NATURAL SUN PROTECTOR SPF50 (TITANIUM DIOXIDE) CREAM [CLEANSIA CORPORATION LTD.]2Legacy NDC, 1 package rows20100901_fb37c4f5-2319-4577-a6b0-c6782b4f9c2f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
TITANIUMACTIVE MOIETYD1JT611TNE2

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
45167-04045167-040-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
4b308335-55a5-486f-ae21-9e598a284275fb37c4f5-2319-4577-a6b0-c6782b4f9c2f2010-09-01Exact identifier
spl id: 4b308335-55a5-486f-ae21-9e598a284275
spl set id: fb37c4f5-2319-4577-a6b0-c6782b4f9c2f

Reported adverse events (FAERS/openFDA)#

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