OXALIS 10 gel

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

Wirkstoff:

OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (OXALIS ACETOSELLA LEAF - UNII:U1W3U02EW0)

Verfügbar ab:

Uriel Pharmacy Inc.

INN (Internationale Bezeichnung):

OXALIS MONTANA LEAF

Zusammensetzung:

OXALIS MONTANA LEAF 1 [hp_X] in 1 g

Verabreichungsweg:

TOPICAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

Directions: FOR TOPICAL USE ONLY. Use: Temporary relief of cramps.

Berechtigungsstatus:

unapproved homeopathic

Fachinformation

OXALIS 10- OXALIS 10 GEL
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._
----------
OXALIS 10
Directions: FOR TOPICAL USE ONLY.
Apply to skin as needed. Under age 2: Consult a doctor.
Active Ingredient: 100 gm contains: 10 gm Oxalis (Wood sorrel) 1X
Inactive Ingredients: Distilled water, Glycerin, Sodium alginate,
Lavender oil, Grapefruit seed extract,
Sorbic acid, Tea tree oil
Use: Temporary relief of cramps.
KEEP OUT OF REACH OF CHILDREN.
Warnings: FOR EXTERNAL USE ONLY.
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, if
conditions worsen or persist, or accidental ingestion occurs. If
pregnant or nursing, consult a doctor
before use. Avoid contact with eyes. Do not use if safety seal is
broken or missing.
Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI
53120 www.urielpharmacy.com
OXALIS 10
oxalis 10 gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:48 9 51-710 2
ROUTE OF ADMINISTRATION
TOPICAL
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
1 [hp_X]
in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
Uriel Pharmacy Inc.
GLYCERIN (UNII: PDC6 A3C0 OX)
SO DIUM ALGINATE (UNII: C26 9 C4G2ZQ)
LAVENDER O IL (UNII: ZBP1YXW0 H8 )
SO RBIC ACID (UNII: X0 45WJ9 8 9 B)
CITRUS PARADISI SEED (UNII: 12F0 8 8 74Y7)
TEA TREE O IL (UNII: VIF56 5UC2G)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:48 9 51-710 2-5
6 0 g in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct
0 9 /0 1/20 0 9
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH