ELDEEN AGE TWENTY ONE MICRO THERAPY PROGRAM

Manufacturer
Small Lab Co., Ltd.
Effective date
2023-09-06
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:26:30

Label at a glance#

ProductELDEEN AGE TWENTY ONE MICRO THERAPY PROGRAM
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SODIUM HYALURONATE

INACTIVE INGREDIENT SECTION

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

ROLLER: WATER, SODIUM HYALURONATE, ALGIN, 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. Take a roller out and connect it to the its handle

2. For 5~10 minutes, do massage using the roller handle.

3. Apply an adequate amount of serum on all of your face smoothly.

4. To get better effect, applying the serum before rolling.

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
71184-6000-12023-09-06C16284748780-1d6a99b39-c3ee-a426-e053-dadaa90af4c27ac2663f-f3a5-8e96-e053-2a91aa0a9178
71184-6000-12022-01-28C16284748780-1d6a99b39-c3ee-a426-e053-dadaa90af4c27ac2663f-f3a5-8e96-e053-2a91aa0a9178

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
71184-400071184-4000-1
71184-500071184-5000-1
71184-600071184-6000-1

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-dd85-58ed-e063-6394a90a22637ac2663f-f3a5-8e96-e053-2a91aa0a91782023-09-06WarningsExact identifier
spl id: 04ab53f7-dd85-58ed-e063-6394a90a2263
spl set id: 7ac2663f-f3a5-8e96-e053-2a91aa0a9178

Reported adverse events (FAERS/openFDA)#

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