Label: SNORESTOP NASOSPRAY 60- strychnos nux-vomica seed,atropa belladonna,ephedra distachya flowering twig,goldenseal,potassium dichromate,teucrium marum,histamine dihydrochloride liquid liquid
- NDC Code(s): 61152-199-99
- Packager: Green Pharmaceuticals 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.
Drug Label Information
Updated June 16, 2022
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- Official Label (Printer Friendly)
- Ingredients:
- Base:
- Directions:
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Directions: Children over 5 years of age and Adults.
Shake before use. 1. Remove cap and safety clip. 2. Prime by placing nozzle between first and second finger with thumb on the bottom of the bottle. Pump sprayer firmly and quickly until a fine spray appears. 3. Insert spray tip into one nostril, pointing the tip toward the back of the nose. Spray quickly while breathing in through your nose. Clean tip of nozzle after each use and replace cap. Store at room temperatur. May be used up to 4 times per day. Please discard 6 months after first use.
For Maximum Results, use in conjunction with SnoreStop FastTabs or SnoreStop Extinguisher.
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Warnings:
Use only as directed. Keep this out of reach of children. Do not use on children under 5 years of age. If pregnant or breastfeeding, ask a physician before use. This product does not treat sleep apnea. For sleep apnea, consult with a specialist. If symptoms worsen after 14 days, discontinue use and ask a physician for help.
- Comments or Questions?
- Keep out of reach of children.
- Uses:
- NasoSpray 60
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INGREDIENTS AND APPEARANCE
SNORESTOP NASOSPRAY 60
strychnos nux-vomica seed,atropa belladonna,ephedra distachya flowering twig,goldenseal,potassium dichromate,teucrium marum,histamine dihydrochloride liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61152-199 Route of Administration NASAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 6 [hp_X] in 9 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 6 [hp_X] in 9 mL EPHEDRA DISTACHYA FLOWERING TWIG (UNII: R55VQ87DP3) (EPHEDRA DISTACHYA FLOWERING TWIG - UNII:R55VQ87DP3) EPHEDRA DISTACHYA FLOWERING TWIG 6 [hp_X] in 9 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 6 [hp_X] in 9 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_X] in 9 mL TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM 6 [hp_X] in 9 mL N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDE (UNII: S6S98U0517) (HISTAMINE - UNII:820484N8I3) N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDE 12 [hp_X] in 9 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM (UNII: 7N6JUD5X6Y) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM CHLORIDE (UNII: 660YQ98I10) POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM PHOSPHATE (UNII: SE337SVY37) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61152-199-99 9 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/19/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/18/2012 Labeler - Green Pharmaceuticals Inc. (937749265) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations HomeoCare Laboratories, Inc. 088248828 manufacture(61152-199) Establishment Name Address ID/FEI Business Operations Green Pharmaceuticals Inc. 937749265 label(61152-199) Establishment Name Address ID/FEI Business Operations Coastal Contract Packaging 137341611 pack(61152-199)