Indications and uses
Indication and Usage: After skincare, apply appropriate amount on all over the face.
MOIST MOISTURE CC
- Manufacturer
- Seindni Co.,ltd | Cosmax, Inc.
- Effective date
- 2018-12-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:57:34
Label at a glance#
ProductMOIST MOISTURE CC
Active ingredientOCTINOXATE, Titanium Dioxide, OCTISALATE
Label structure8 sections
Dosage and administration
Dosage and Administration : Take an adequate amount of this product.
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active Ingredients: Ethylhexyl Methoxycinnamate 6.7%, Titanium Dioxide 4.2%, Ethylhexyl Salicylate 2.5%
INACTIVE INGREDIENT
Inactive Ingredients:
Water,Butylene Glycol,Glycerin,Cyclopentasiloxane, Cyclohexasiloxane,Niacinamide,Dicaprylyl Carbonate,Cetyl Ethylhexanoate,Octyldodecanol,Diethylamino Hydroxybenzoyl Hexyl Benzoate, Diphenylsiloxy Phenyl Trimethicone,Mica (CI 77019),Triceteareth-4 Phosphate,Glycol Stearate, Phenoxyethanol Glyceryl Stearate,Potassium Cetyl
Phosphate,PEG-2 Stearate,PEG-100 Stearate,PEG-10 Dimethicone,Carbomer,Triethanolamine,Silica,Aluminum Hydroxide,Stearic Acid,Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Fragrance(Parfum),Isohexadecane,Ethylhexylglycerin, Triethoxycaprylylsilane,Xanthan Gum,Adenosine,Polysorbate 80,Iron Oxides (CI 77492),Disodium EDTA, Iron Oxides (CI 77491),Ultramarines (CI 77007), Snail Secretion Filtrate,Melissa Officinalis Leaf Extract, Malva Sylvestris (Mallow) Extract,Achillea Millefolium Extract,Alchemilla Vulgaris Extract, Primula Veris Extract,Mentha Piperita (Peppermint) Leaf Extract,Veronica Officinalis Extract,Vinegar Lavandula Angustifolia (Lavender) Extract,Rosmarinus Officinalis (Rosemary) Leaf Extract,Melaleuca Alternifolia (Tea Tree) Leaf Extract,Saccharomyces Ferment Filtrate
PURPOSE
Purpose: Sunscreen
WARNINGS
Warning:
1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
2. you are banned to use it on the part where you have a scar, eczema, or dermatitis.
3. In case of getting it into your eyes, you have to wash it immediately.
KEEP OUT OF REACH OF CHILDREN
Keep out of reach of Children: Keep out of reach of babies and children
INDICATIONS AND USAGE
Indication and Usage: After skincare, apply appropriate amount on all over the face.
DOSAGE AND ADMINISTRATION
Dosage and Administration : Take an adequate amount of this product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69072-020-01 | 2023-01-30 | C162847 | 48780-1 | f386c649-ce0a-0266-e053-dadaa90a7c1a | eae95288-0612-420e-a6dc-0f8a9694c133 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69072-020-01 | MOIST MOISTURE CC | 30 mL in 1 CARTON | CREAM | 30 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OCTINOXATE | ACTIVE INGREDIENT | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE INGREDIENT | 4X49Y0596W | 1 | |
| Titanium Dioxide | ACTIVE INGREDIENT | 15FIX9V2JP | 1 | |
| OCTINOXATE | ACTIVE MOIETY | 4Y5P7MUD51 | 1 | |
| OCTISALATE | ACTIVE MOIETY | 4X49Y0596W | 1 | |
| TITANIUM DIOXIDE | ACTIVE MOIETY | 15FIX9V2JP | 1 | |
| Butylene Glycol | INACTIVE INGREDIENT | 3XUS85K0RA | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- MOIST MOISTURE CC
- OCTINOXATE, Titanium Dioxide, OCTISALATE
- OCTINOXATE
- Titanium Dioxide
- OCTISALATE
- Water
- Butylene Glycol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69072-020 | 69072-020-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| Titanium Dioxide | 15FIX9V2JP | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| Water | 059QF0KO0R | IACT |
| Butylene Glycol | 3XUS85K0RA | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| Butylene Glycol | BUTYLENE GLYCOL | 3XUS85K0RA | SYSTEM / TOPICAL | 1400 mg | ||
| Butylene Glycol | BUTYLENE GLYCOL | 3XUS85K0RA | SYSTEM / TRANSDERMAL | 8.12 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5bb9c063-8819-4e8b-845e-326fbd4e4d31 | eae95288-0612-420e-a6dc-0f8a9694c133 | 2018-12-10 | Warnings | 5bb9c063-8819-4e8b-845e-326fbd4e4d31 eae95288-0612-420e-a6dc-0f8a9694c133 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.