ELDEEN AGE TWENTY ONE MifitPatch and Serum

Manufacturer
Small Lab Co., Ltd.
Effective date
2023-09-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:26:29

Label at a glance#

ProductELDEEN AGE TWENTY ONE MifitPatch and Serum
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SODIUM HYALURONATE

INACTIVE INGREDIENT SECTION

SERUM: WATER, ALGIN, GLYCERIN, BETAINE, ETC.

PATCH: WATER, CELLULOSE GUM, GLYCERIN, TREHALOSE, ETC.

OTC - PURPOSE SECTION

Skin Care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children

INDICATIONS & USAGE SECTION

1. After cleansing, keep your skin clearly.

2. Apply serum on your face and massage with your finger lightly.

3. Carefully remove both films. (white and transparence)

4. Stick the patch to target areas of concern (under eyes, smile, and frown lines) and gently press down on the patch for 2-3 minutes.

5. Leave in place for 2 hours or more.

WARNINGS SECTION

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71184-3000-12023-09-06C16284748780-1d6a99b39-6aae-a426-e053-dadaa90af4c27aad7402-0ee4-29cc-e053-2991aa0a6544
71184-3000-12022-01-28C16284748780-1d6a99b39-6aae-a426-e053-dadaa90af4c27aad7402-0ee4-29cc-e053-2991aa0a6544

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71184-100071184-1000-1
71184-200071184-2000-1
71184-300071184-3000-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
04ab53f7-dd84-58ed-e063-6394a90a22637aad7402-0ee4-29cc-e053-2991aa0a65442023-09-06WarningsExact identifier
spl id: 04ab53f7-dd84-58ed-e063-6394a90a2263
spl set id: 7aad7402-0ee4-29cc-e053-2991aa0a6544

Reported adverse events (FAERS/openFDA)#

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