TEREBINTHINA- turpentine liquid

国: アメリカ合衆国

言語: 英語

ソース: NLM (National Library of Medicine)

有効成分:

TEREBINTHINA

から入手可能:

Washington Homeopathic Products

投与経路:

ORAL

処方タイプ:

OTC DRUG

適応症:

To relieve urinary symptoms. Indications: TEREBINTHINA Urinary symptoms If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

認証ステータス:

unapproved homeopathic

製品の特徴

TEREBINTHINA- TURPENTINE LIQUID
WASHINGTON HOMEOPATHIC PRODUCTS
_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._
----------
DRUG FACTS
ACTIVE INGREDIENTS
TEREBINTHINA
USES
To relieve urinary symptoms.
KEEP OUT OF REACH OF CHILDREN
Keep this and all medicines out of reach of children.
INDICATIONS
Indications:
TEREBINTHINA Urinary symptoms
STOP USE AND ASK DOCTOR
If symptoms persist/worsen or if pregnant/nursing, consult your
practitioner.
DIRECTIONS
Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2
dose. Repeat at greater intervals as
condition subsides. Or as directed bya lic. practitioner.
INACTIVE INGREDIENTS
Sucrose/Lactose
PRINCIPAL DISPLAY PANEL
The OTC potency range of TEREBINTHINA is 2x–30x, 1c–30c, 200c, 1m,
10m, 50m, and CM.
Availability is subject to change.
All WHP single remedies are made to order; thus, the labels are
printed on the same label stock, as the
orders are filled.
‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on
the label depending on customer choice.
Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml,
and 100ml.
TEREBINTHINA
turpentine liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:719 19 -6 6 9
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
TURPENTINE (UNII: XJ6 RUH0 O4G) (TURPENTINE - UNII:XJ6 RUH0 O4G)
TURPENTINE
30 [hp_C] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M)
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:719 19 -6 6 9 -
0 7
15 mL in 1 VIAL, GLASS; Type 0 : No t a Co mbinatio n Pro duct
0 5/17/20 11
2
NDC:719 19 -6 6 9 -
0 8
30 mL in 1 VIAL, GLASS; Type 0 : No t a Co mbinatio n Pro duct
0 5/17/20 11
3
NDC:719 19 -6 6 9 -
0 9
50 mL in 1 BOTTLE, GLASS; Type 0 : No t