Label: GUNA-TF PAPILLOMA- human papillomavirus capsule, gelatin coated
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Contains inactivated NDC Code(s)
NDC Code(s): 17089-281-10 - Packager: Guna spa
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 Label Information
Updated March 31, 2010
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INGREDIENTS AND APPEARANCE
GUNA-TF PAPILLOMA
human papillomavirus capsule, gelatin coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17089-281 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (HUMAN PAPILLOMAVIRUS - UNII:23CVL7WF4J) HUMAN PAPILLOMAVIRUS 7 [hp_X] in 4600 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) 4048 mg in 4600 mg MAGNESIUM STEARATE (UNII: 70097M6I30) 92 mg in 4600 mg Product Characteristics Color white (white) Score 2 pieces Shape OVAL (Capsule) Size 18mm Flavor Imprint Code na Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17089-281-10 1 in 1 BOX 1 4600 mg in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/16/2008 Labeler - Guna spa (430538264) Establishment Name Address ID/FEI Business Operations Guna spa 430538264 manufacture