FORMICA OXALIS liquid

Ülke: ABD

Dil: İngilizce

Kaynak: NLM (National Library of Medicine)

Aktif bileşen:

OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (OXALIS ACETOSELLA LEAF - UNII:U1W3U02EW0), FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5)

Mevcut itibaren:

Uriel Pharmacy Inc.

INN (International Adı):

OXALIS MONTANA LEAF

Kompozisyon:

OXALIS MONTANA LEAF 3 [hp_X] in 1 mL

Uygulama yolu:

ORAL

Reçete türü:

OTC DRUG

Terapötik endikasyonlar:

Directions: FOR ORAL USE. Use: Temporary relief of sore muscles.

Yetkilendirme durumu:

unapproved homeopathic

Ürün özellikleri

FORMICA OXALIS- FORMICA OXALIS 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._
----------
FORMICA OXALIS
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then swallow.
Active Ingredients: Oxalis (Wood sorrel) 3X, Formica (Red wood ant) 5X
Inactive Ingredients: Water, Salt
Use: Temporary relief of sore muscles.
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
FORMICA OXALIS
formica oxalis liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:48 9 51-40 8 9
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
O XALIS ACETO SELLA LEAF (UNII: U1W3U0 2EW0 ) (OXALIS ACETOSELLA LEAF
-
UNII:U1W3U0 2EW0 )
OXALIS ACETOSELLA
LEAF
3 [hp_X]
in 1 mL
FO RMICA RUFA (UNII: 55H0 W8 3JO5) (FORMICA RUFA - UNII:55H0 W8 3JO5)
FORMICA RUFA
5 [hp_X]
in 1 mL
Uriel Pharmacy Inc.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE MARKETING END DATE
1
NDC:48 9 51-40 8 9 -
1
10 in 1 BOX
0 9 /0 1/20 0 9
1
1 mL in 1 AMPULE; Type 1: Co nvenience Kit o f Co -Package
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
unappro ved ho meo pathic
0 9 /0 1/20 0 9
LABELER -
Uriel Pharmacy Inc. (043471163)
ESTABLISHMENT
NAME
AD D RE S S
ID/FEI
BUSINE SS OPE RATIONS
Uriel Pharmacy Inc.
0 4347116 3
ma nufa