Label: SNORE CONTROL- bromium, chamomilla, cinchona officinalis, cuprum metallicum, helleborus niger, laurocerasus, nux vomica, phosphoricum acidum, rhus tox, silicea, stramonium, zincum metallicum. liquid
- NDC Code(s): 57955-5122-2
- Packager: King Bio Inc.
- 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 December 6, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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OTHER SAFETY INFORMATION
Other information
Tamper resistant for your protection.
Use only if safety seal is intact.
Keep carton for complete drug facts and product information.
Questions? Call 866.298.2740
King Bio, Inc. 3 Westside Drive
Asheville, NC 2806 USA
FDA Reg. #1053442
For latest product information and instructions: www.DrKings.com
Reference image:Snore Control.jpg
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Inactive Ingredients
Citrus Extract (ascorbic acid, citric acid, citrus aurantium amara fruit extract, citrus aurantium sinensis peel extract, citrus reticulata fruit extact, demineralized water, glycerin, lactic acid), Honeysuckle (Lonicera japonica), Polylysine, Purified Water, Shagbark Hickory (Carya Ovata) Bark Extract, Steviol (Steviol Glycosides).
Reference image:Snore Control.jpg
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Active ingredients
Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM
potencies.Bromium, Chamomilla, Cinchona officinalis, Cuprum metallicum, Helleborus niger, Laurocerasus, Nux vomica, Phosphoricum acidum, Rhus tox,
Silicea, Stramonium, Zincum metallicum.HPUS indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.
Reference image:Snore Control.jpg
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Uses
Uses for temporary relief of symptoms related to snoring:
Slow, labored breathing
Stuffy nose, especially at night
Heaviness of chest
Dry cough
as per various homeopathic materia medicas. Claims based
on traditional homeopathic practice, not accepted medical
evidence. These uses have not been evaluated by the FDA,
and product has not been clinically tested.Reference image:Snore Control.jpg
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Warnings
Stop use and consult a physician if symptoms worsen or
persist for more than 7 days.If pregnant or breast-feeding, ask a healthcare professional
before use.Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center immediately.
Reference image:Snore Control.jpg
- KEEP OUT OF REACH OF CHILDREN
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PURPOSE
Active ingredients Purpose †
Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM
potencies.Bromium ................................... jerking and starting during sleep
Chamomilla .....................................................tightness of chest
Cinchona officinalis ...................................slow, labored breathing
Cuprum metallicum .............................................spasms of chest
Helleborus niger..............................................irregular respiration
Laurocerasus ...................................spasmodic tickling, dry cough
Nux vomica ....................................stuffy nose, especially at night
Phosphoricum acidum.........................................difficult breathing
Rhus tox .................................heaviness of chest, bronchial cough
Silicea.....................................................coughs when lying down
Stramonium............................................................ deep snoring
Zincum metallicum .....................................................hoarseness**“HPUS” indicates the active ingredients are in the official
Homeopathic Pharmacopeia of the United States.Reference image:Snore Control.jpg
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SNORE CONTROL
bromium, chamomilla, cinchona officinalis, cuprum metallicum, helleborus niger, laurocerasus, nux vomica, phosphoricum acidum, rhus tox, silicea, stramonium, zincum metallicum. liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-5122 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G) BROMINE 10 [hp_X] in 59 mL MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ) MATRICARIA CHAMOMILLA WHOLE 10 [hp_X] in 59 mL CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 10 [hp_X] in 59 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 10 [hp_X] in 59 mL HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815) HELLEBORUS NIGER ROOT 10 [hp_X] in 59 mL PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757) (PRUNUS LAUROCERASUS LEAF - UNII:F26P2D4757) PRUNUS LAUROCERASUS LEAF 10 [hp_X] in 59 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 10 [hp_X] in 59 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 10 [hp_X] in 59 mL TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 10 [hp_X] in 59 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 10 [hp_X] in 59 mL DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM 10 [hp_X] in 59 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 10 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) ORANGE PEEL (UNII: TI9T76XD44) CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY) CARYA OVATA BARK (UNII: X765CF609L) STEVIOL (UNII: 4741LYX6RT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-5122-2 1 in 1 CARTON 12/06/2022 1 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/06/2022 Labeler - King Bio Inc. (617901350) Registrant - King Bio Inc. (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc. 617901350 manufacture(57955-5122) , api manufacture(57955-5122)