Label: KIDS ALLERGY EYE RELIEF- apis and euphrasia and pulsatilla and sabadilla solution/ drops
- NDC Code(s): 59262-361-11
- Packager: Similasan Corporation
- 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.
Drug Label Information
Updated September 30, 2020
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses:
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Warnings:
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For external use only.
- Children under 2 years of age should be seen by a physician.
- According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).
- To avoid contamination do not touch the tip of the bottle to any surface.
- To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.
- Contact wearers: consult a physician prior to using.
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For external use only.
- Directions:
- Other Information:
- Inactive Ingredients:
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIDS ALLERGY EYE RELIEF
apis and euphrasia and pulsatilla and sabadilla solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-361 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 6 [hp_X] in 0.45 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 0.45 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_X] in 0.45 mL SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED 6 [hp_X] in 0.45 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) WATER (UNII: 059QF0KO0R) SILVER SULFATE (UNII: 8QG6HV4ZPO) SODIUM NITRATE (UNII: 8M4L3H2ZVZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-361-11 1 in 1 BOX 07/02/2013 1 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/02/2013 Labeler - Similasan Corporation (111566530)