OXALIS 5- oxalis 5 cream 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. ------Directions: FOR TOPICAL USE ONLY. Apply to skin as needed. Under age 2: Consult a doctor. Active Ingredient: Oxalis (Wood sorrel) 5X Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Potassium sorbate, Frankincense oil, Myrrh oil, Grapefruit seed extract Use: Temporary relief of cramps. KEEP OUT OF REACH OF CHILDREN. Warnings: FOR EXTERNAL USE ONLY. 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. Natural ingredients may cause color and/or scent variation. Questions? Call 866.642.2858 Made by with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com
OXALIS 5 oxalis 5 cream
Product Information Product T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:48 9 51-710 6 Route of Administration TOPICAL
Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength O XALIS ACETO SELLA LEAF (UNII: U1W3U0 2EW0 ) (OXALIS ACETOSELLA LEAF - OXALIS ACETOSELLA 5 [hp_X] UNII:U1W3U0 2EW0 ) LEAF in 1 g
Inactive Ingredients Ingredient Name Strength WATER (UNII: 0 59 QF0 KO0 R) STEARIC ACID (UNII: 4ELV7Z6 5AP) ISO PRO PYL MYRISTATE (UNII: 0 RE8 K4LNJS) LAVENDER O IL (UNII: ZBP1YXW0 H8 ) CETYL ALCO HO L (UNII: 9 36 JST6 JCN) PO LYO XYL 4 0 STEARATE (UNII: 13A4J4NH9 I) STEARYL ALCO HO L (UNII: 2KR8 9 I4H1Y) XANTHAN GUM (UNII: TTV12P4NEE) PO TASSIUM SO RBATE (UNII: 1VPU26 JZZ4) FRANKINCENSE O IL (UNII: 6 7ZYA5T0 2K) MYRRH O IL (UNII: H74221J5J4) CITRUS PARADISI SEED (UNII: 12F0 8 8 74Y7)
Product Characteristics Color white Score Shape Siz e Flavor Imprint Code Contains
Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48 9 51-710 6 -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 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 Addre ss ID/FEI Busine ss Ope rations Uriel Pharmacy Inc. 0 4347116 3 manufacture(48 9 51-710 6 )
Revised: 8/2017 Uriel Pharmacy Inc.