FDA.reportPublic FDA data

IASO CONTROL MAKE UP BASE 60

Manufacturer
IASO Inc | Kolmar Korea Co., Ltd
Effective date
2018-03-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:01:05

Label at a glance#

ProductIASO CONTROL MAKE UP BASE 60
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

zinc oxide


INACTIVE INGREDIENT SECTION

water, cyclopentasiloxane, ethylhexyl methoxycinnamate, glycerin, ethylhexyl salicylate, peg-10 dimethicone, dipropylene glycol, cyclomethicone, betaine, disteardimonium hectorite, hexyl laurate, magnesium sulfate, talc, aluminum hydroxide, aluminum stearate, methylparaben palmitic acid, acrylates/dimethicone copolymer, fragrance, imidazolidinyl urea, chromium, oxide greens, dimethicone/vinyl dimethicone crosspolymer, methicone, propylparaben, silica, tocopheryl acetate, butylparaben, distearyldimonium chloride, glycosyl trehalose, hydrogenated starch hydrolysate, dimethicone, ci 77492, aloe barbadensis leaf juice, bisabolol, camellia sinensis leaf extract, hydrolyzed lupine protein, morus nigra leaf ext, panax ginseng root ext, squalane, portulaca oleracea extract, rosa canina fruit oil, rosa centifolia flower water, rosemary leaf ext, stearyl glycyrrhetinate


OTC - PURPOSE SECTION

skin protectant


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

pump a small amount on the fingertips and apply evenly to the entire face before using a foundation or powder pact


WARNINGS SECTION

- Stop using if sensitivities occurs and consult with dermatologist
- sensitivities such as red marks, intumescence, urtication, irritation during use
-Have sensitivities as above on applied part by direct sun ray
- Do not store at high and low temperatures and avoid sunlight.


DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75847-1712-12024-06-28C16284748780-1d6a99b39-9cd6-a426-e053-dadaa90af4c2Drug Facts
75847-1712-12022-01-28C16284748780-1d6a99b39-9cd6-a426-e053-dadaa90af4c2Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
ALUMINUM HYDROXIDEINACTIVE INGREDIENT5QB0T2IUN01
CYCLOMETHICONEINACTIVE INGREDIENTNMQ347994Z1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
SQUALENEINACTIVE INGREDIENT7QWM220FJH1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75847-171275847-1712-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
CYCLOMETHICONENMQ347994ZIACT
SQUALENE7QWM220FJHIACT
ZINC OXIDESOI2LOH54ZACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0CREAM / TOPICAL5 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0TABLET / ORAL50 mgExact identifier — unii candidate
4 equally ranked IID candidates
CYCLOMETHICONECYCLOMETHICONENMQ347994ZAEROSOL, FOAM / TOPICAL376 mgExact identifier — unii candidate
5 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0CAPSULE / ORALNAExact identifier — unii candidate
4 equally ranked IID candidates
CYCLOMETHICONECYCLOMETHICONENMQ347994ZLOTION / TOPICAL3510 mgExact identifier — unii candidate
5 equally ranked IID candidates
CYCLOMETHICONECYCLOMETHICONENMQ347994ZCREAM, AUGMENTED / TOPICAL389 mgExact identifier — unii candidate
5 equally ranked IID candidates
ALUMINUM HYDROXIDEALUMINUM HYDROXIDE5QB0T2IUN0OINTMENT / TOPICALNAExact identifier — unii candidate
4 equally ranked IID candidates
CYCLOMETHICONECYCLOMETHICONENMQ347994ZCREAM / TOPICAL358 mgExact identifier — unii candidate
5 equally ranked IID candidates
CYCLOMETHICONECYCLOMETHICONENMQ347994ZSOLUTION / TOPICAL11.57 %w/vExact identifier — unii candidate
5 equally ranked IID candidates

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
1bcec96e-54cd-8c44-e063-6294a90ace9e84f5060a-273c-483f-8c02-c72af449447d2024-06-26WarningsExact identifier
spl set id: 84f5060a-273c-483f-8c02-c72af449447d

Reported adverse events (FAERS/openFDA)#

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