RAMOSU HYALURONIC ACID SOLUTION 100- hyaluronate sodium liquid

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Principio attivo:

HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)

Commercializzato da:

RaMoSu

Via di somministrazione:

TOPICAL

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

for skin protectant apply proper amount to the skin

Stato dell'autorizzazione:

unapproved drug other

Scheda tecnica

RAMOSU HYALURONIC ACID SOLUTION 100- HYALURONATE SODIUM LIQUID
RAMOSU
_Disclaimer: This drug has not been found by FDA to be safe and
effective, and this labeling has not been_
_approved by FDA. For further information about unapproved drugs,
click here._
----------
DRUG FACTS
hyaluronate sodium
water
for skin protectant
keep out of reach of the children
apply proper amount to the skin
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
for external use only
RAMOSU HYALURONIC ACID SOLUTION 100
hyaluronate sodium liquid
PRODUCT INFORMATION
RaMoSu
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:70 46 5-0 0 0 3
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HYALURO NATE SO DIUM (UNII: YSE9 PPT4TH) (HYALURONIC ACID -
UNII:S270 N0 TRQY)
HYALURONATE
SODIUM
10 0 g
in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:70 46 5-0 0 0 3-1
10 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
unappro ved drug o ther
0 2/0 4/20 16
LABELER -
RaMoSu (689055324)
REGISTRANT -
RaMoSu (689055324)
ESTABLISHMENT
NAME
AD D RE S S
ID/FEI
BUSINE SS OPE RATIONS
RaMo Su
6 8 9 0 55324
ma nu