APIS LEVISTICUM liquid

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

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Last ned Preparatomtale (SPC)
30-10-2023

Aktiv ingrediens:

APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z), LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE ROOT - UNII:46QZ19OEX8)

Tilgjengelig fra:

Uriel Pharmacy Inc.

INN (International Name):

APIS MELLIFERA

Sammensetning:

APIS MELLIFERA 3 [hp_X] in 1 mL

Administreringsrute:

ORAL

Resept typen:

OTC DRUG

Indikasjoner:

Directions: FOR ORAL USE.

Autorisasjon status:

unapproved homeopathic

Preparatomtale

                                APIS LEVISTICUM- APIS LEVISTICUM 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._
----------
APIS LEVISTICUM
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredients: Apis (Honeybee) 3X, Levisticum (Lovage) 3X
Inactive Ingredients: Water, Salt
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
Made by Uriel, East Troy, WI 53120
shopuriel.com
APIS LEVISTICUM
apis levisticum liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-1058
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)
APIS MELLIFERA
3 [hp_X]
in 1 mL
LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE
ROOT - UNII:46QZ19OEX8)
LEVISTICUM
OFFICINALE ROOT
3 [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-
1058-1
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(48951-1058)
Revised: 10/2023
                                
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