IASO SMART PACT 23

Manufacturer
IASO Inc | Kolmar Korea Co., Ltd
Effective date
2018-03-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:01:04

Label at a glance#

ProductIASO SMART PACT 23
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

zinc oxide


INACTIVE INGREDIENT SECTION

mica, talc, titanium dioxide, silica, dimethicone, boron nitride, dimethicone/vinyl dimethicone crosspolymer, ci 77492, zinc myristate, cetyl caprylate, vinyl dimethicone/methicone silsesquioxane crosspolymer, aluminium hydroxide, stearic acid, aluminum starch octenylsuccinate, aluminum dimyristate, ci 77491, glyceryl rosinate, methicone, octyldodecyl myristate, c9-15 fluoroalcohol phosphate, magnesium myristate, methylparaben, dimethicone/methicone copolymer, fragrance, tocopheryl acetate, trimethylsiloxysilicate, ci 77499, propylparaben, lycium chinense fruit ext, cornus officinalis fruit ext, schizandra chinensis fruit ext


OTC - PURPOSE SECTION

skin protectant


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply the powder to the attached puff and gently pat onto the face following the application of IASO triple protection bb spf 30 pa++ or essence liquid foundation


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
75847-0004-12024-06-28C16284748780-1d6a99b39-4ec3-a426-e053-dadaa90af4c2Drug Facts
75847-0004-12022-01-28C16284748780-1d6a99b39-4ec3-a426-e053-dadaa90af4c2Drug Facts

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
75847-000475847-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
1bcec96e-54d9-8c44-e063-6294a90ace9e67327bf2-eca8-44fa-e053-2a91aa0ab9092024-06-26WarningsExact identifier
spl set id: 67327bf2-eca8-44fa-e053-2a91aa0ab909

Reported adverse events (FAERS/openFDA)#

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