Label: SILICA- silica powder
- NDC Code(s): 48951-8317-7
- Packager: Uriel Pharmacy Inc
- Category: HUMAN OTC DRUG LABEL
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.
Updated July 24, 2017
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Uses: To promote skin elasticity and strengthen hair and nails.Close
- Dosage & Administration
Directions: Take regularly before meals with a small amount of water. Ages 12 and older: 1 tsp. Ages 2-11: 1/2 tsp. Under age 2: Ask a doctor.Close
- OTC-Active Ingredient
Active Ingredients: Stannum met. (Metallic tin) 3X, Cinis equiseti (Ash of horsetail herb) 5X, Cinis quercus (Decoction of oak bark ash) 9X, Cor (Bovine heart) 9X, Hepar (Bovine liver) 9X, Pancreas (Bovine pancreas) 9X, Pulmo (Bovine lung) 9X, Quercus (Oak) 9X, Renes (Bovine kidneys) 9X, Mesenchyme (Porcine embryonic connective tissue) 11XClose
- Uses: To promote skin elasticity and strengthen hair and nails.
- Inactive Ingredient
Inactive Ingredients: Lactose, Bee pollen, Diatomaceous earth, Anise oil, Mesenchyme, Pancreas, Pulmo, Cor, Renes.Close
- Keep out of reach of children
KEEP OUT OF REACH OF CHILDREN.Close
- Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.
Warnings: Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.Close
- Ask doctor section
Consult your doctor if you are lactose intolerant.Close
- Pregnancy or breast feeding section
If you are pregnant or nursing, consult a doctor before use.Close
- Questions section
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East Troy, WI 53120
Questions or comments?
Please call 1.866.642.2858
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- INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8317 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP 5 [hp_X] WHITE OAK BARK (UNII: 93LP7Y8EGT) (WHITE OAK BARK - UNII:93LP7Y8EGT) WHITE OAK BARK 9 [hp_X] MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER 9 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) POLLEN (UNII: 3729L8MA2C) ANISE OIL (UNII: 6Y89129C8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8317-7 1 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009 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(48951-8317)