Label: OXALIS 5- oxalis montana leaf cream
- NDC Code(s): 48951-7106-5
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- INDICATIONS & USAGE
Directions: FOR TOPICAL USE ONLY.Close
- DOSAGE & ADMINISTRATION
Apply to skin as needed. Under age 2: Consult a doctor.Close
- ACTIVE INGREDIENT
Active Ingredient: Oxalis e pl. tota 3XClose
- INACTIVE INGREDIENT
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 extractClose
Use: Temporary relief of cramps.Close
- KEEP OUT OF REACH OF CHILDREN
KEEP OUT OF REACH OF CHILDREN.Close
Warnings: FOR EXTERNAL USE ONLY.Close
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 866.642.2858Close
Made by with care by Uriel, East Troy, WI 53120
- INGREDIENTS AND APPEARANCE
oxalis 5 cream
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:48951-7106 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXALIS MONTANA LEAF (OXALIS MONTANA LEAF) OXALIS MONTANA LEAF 5 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength WATER STEARIC ACID ISOPROPYL MYRISTATE LAVENDER OIL CETYL ALCOHOL POLYOXYL 40 STEARATE STEARYL ALCOHOL XANTHAN GUM POTASSIUM SORBATE FRANKINCENSE OIL MYRRH OIL CITRUS PARADISI SEED Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-7106-5 60 g in 1 TUBE 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(48951-7106)