Label: DRY EYES- pulsatilla vulgaris - silicon dioxide - sulfur pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 68428-006-14 - Packager: Washington Homeopathic Products
- 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 October 15, 2010
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- ACTIVE INGREDIENTS
- USES
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS
- STOP USE AND ASK DOCTOR
- DIRECTIONS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DRY EYES
pulsatilla vulgaris - silicon dioxide - sulfur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_C] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_C] SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white (white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68428-006-14 300 in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/20/2010 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture