NDC | 71184-4000-1, 71184-5000-1, 71184-6000-1 |
Set ID | 7ac2663f-f3a5-8e96-e053-2a91aa0a9178 |
Category | HUMAN OTC DRUG LABEL |
Packager | Small Lab Co., Ltd. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELDEEN AGE TWENTY ONE MICRO THERAPY PROGRAM
sodium hyaluronate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71184-6000 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71184-6000-1 1 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE, PUMP 30 mL Part 2 8 POUCH 360 mg Part 1 of 2 ELDEEN AGE TWENTY ONE SERUM
sodium hyaluronate liquidProduct Information Item Code (Source) NDC:71184-4000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 0.4298 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71184-4000-1 30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2020 Part 2 of 2 ELDEEN AGE TWENTY ONE MICRO THERAPY ROLLER
sodium hyaluronate patchProduct Information Item Code (Source) NDC:71184-5000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 6.14 g in 100 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71184-5000-1 4 in 1 POUCH 1 45 mg in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2020 Labeler - Small Lab Co., Ltd. (688438425) Registrant - Small Lab Co., Ltd. (688438425) Establishment Name Address ID/FEI Business Operations Small Lab Co., Ltd. 688438425 manufacture(71184-4000, 71184-5000, 71184-6000) , label(71184-4000, 71184-5000, 71184-6000) , pack(71184-4000, 71184-5000, 71184-6000)