Label: STYE RELIEF- apis mellifera - carbon disulfide - pulsatilla vulgaris - silicon dioxide - delphinium staphisagria seed - ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 17312-014-13 - Packager: TRP Company
- 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 15, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
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Uses
Uses*
According to homeopathic indications these ingredients provide temporary relief from symptoms such as:
• Red swollen bumps on the eyelid • Itching, burning or swollen eyelids after serious causes have been ruled out by a physician.
*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. - Purpose
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- WARNINGS
- Do not use:
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions:
- Wash your hands.
- Open the cap and squeeze out approx. 1/8" of the ointment onto your finger tip.
- Gently apply the ointment directly to the stye.
- Replace cap after each use.
- Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use.
- Apply 3-4 times a day.
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SPL UNCLASSIFIED SECTION
Other information
- Non-prescription drug products cannot treat infections.
- There are no known contraindications.
- Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects.
- Store in a cool dark location.
- Keep tube tightly closed.
Stye Relief Homeopathic Sterile Lubricating Eye Ointment are homeopathic dilutions, see www.thereliefproducts.com for details.
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STYE RELIEF
apis mellifera - carbon disulfide - pulsatilla vulgaris - silicon dioxide - delphinium staphisagria seed - ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17312-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 6 [hp_C] in 4 g CARBON DISULFIDE (UNII: S54S8B99E8) (CARBON DISULFIDE - UNII:S54S8B99E8) CARBON DISULFIDE 6 [hp_C] in 4 g PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_C] in 4 g SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 [hp_C] in 4 g DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED 6 [hp_C] in 4 g Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) WHEAT GERM OIL (UNII: 14C97E680P) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17312-014-13 1 in 1 PACKAGE 08/27/2014 1 4 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/01/2011 Labeler - TRP Company (105185719) Registrant - TRP Company (105185719)