ACONITUM E TUB. 30 liquid

Negara: Amerika Serikat

Bahasa: Inggris

Sumber: NLM (National Library of Medicine)

Beli Sekarang

Karakteristik produk Karakteristik produk (SPC)
07-07-2021

Bahan aktif:

ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)

Tersedia dari:

Uriel Pharmacy Inc.

INN (Nama Internasional):

ACONITUM NAPELLUS

Komposisi:

ACONITUM NAPELLUS 30 [hp_X] in 1 mL

Rute administrasi :

ORAL

Jenis Resep:

OTC DRUG

Indikasi Terapi:

Directions: FOR ORAL USE.

Status otorisasi:

unapproved homeopathic

Karakteristik produk

                                ACONITUM E TUB. 30- ACONITUM E TUB. 30 LIQUID
URIEL PHARMACY INC.
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug_
_Administration for safety or efficacy. FDA is not aware of scientific
evidence to support_
_homeopathy as effective._
----------
ACONITUM E TUB. 30
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredient: Aconitum (Monkshood) 30X
Use: Temporary relief of headache.
KEEP OUT OF REACH OF CHILDREN.
.Warnings: Claims based on traditional homeopathic practice, not
accepted medical
evidence. Not FDA evaluated. Do not use if allergic to any ingredient.
Consult a doctor
before use for serious conditions or if conditions worsen or persist.
If pregnant or
nursing, consult a doctor before use.
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120
www.urielpharmacy.com
ACONITUM E TUB. 30
aconitum e tub. 30 liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-9171
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
Uriel Pharmacy Inc.
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS -
UNII:U0NQ8555JD)
ACONITUM
NAPELLUS
30 [hp_X]
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:48951-
9171-1
10 in 1 BOX
09/01/2009
1
1 mL in 1 AMPULE; Type 0: Not a Combination
Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved
homeopathic
09/01/2009
LABELER -
Uriel Pharmacy Inc. (043471163)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Uriel Pharmacy Inc.
043471163
manufacture(48951-9171)
Revised: 7/2021
                                
                                Baca dokumen lengkapnya
                                
                            

Peringatan pencarian terkait dengan produk ini