RESTLESS LEG SYMPTOM RELIEF- arsenicum album, bufo rana, causticum, chamomilla, crotalus horridus, digitalis purpurea, lachesis mutus, lilium tigrinum, pulsatilla, rhus tox, sulphur, tarentula hispana, viscum album and zincum metallicum. liquid

Restless Leg Symptom Relief by

Drug Labeling and Warnings

Restless Leg Symptom Relief by is a Homeopathic medication manufactured, distributed, or labeled by King Bio Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies.

Arsenicum album, Bufo rana, Causticum, Chamomilla, Crotalus horridus, Digitalis purpurea, Lachesis mutus, Lilium tigrinum, Pulsatilla, Rhus tox, Sulphur, Tarentula hispana, Viscum album and Zincum metallicum.

** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″

INDICATIONS & USAGE

Uses † For temporary relief of:

• urge to move the legs
• heaviness
• muscle stiffness
• uneasiness in legs
• leg cramps
• twitching, drawing, jerking legs
• burning sensation

† Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated.

Questions

Restless Leg Symptom Relief

Dr. King's Natural Medicine

Taste free, Pure Water Base

Oral Spray Gluten Free

HOMEOPATHIC 2 fl oz (59 mL)

*Less than 1% Alcohol. Tamper evident for your protection.

King Bio 3 Westside Drive, Asheville, NC 28806 USA

www.DrKings.com
for additional information.

Scan and discover Dr. King's FREE Videos and Home
Healing Techniques to integrate with
this product and optimize your
healing experience.

Warnings

• Stop use and consult a doctor 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

• Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

• Directions: Oral Dose
• Adults and Children over 12:
  • 2 sprays into mouth 3 to 6 times per day
• Children 6-12:
  • 1 spray into mouth 3 to 6 times per day
• Children under 6:
  • Do not use in children under 6, unless directed to by a doctor

OTHER SAFETY INFORMATION

Other information

Tamper evident for your protection. Use only if safety seal is intact.

Inactive Ingredients

Citric acid, Potassium sorbate, and USP purified water.

PURPOSE

Active ingredients                                     Purpose †

Equal volumes of each HPUS** ingredient in 10X,
30X, and 1LM potencies.

Arsenicum album ..........................restlessness, leg cramps
Bufo rana ...........................................................stiffness
Causticum..........................................restless legs at night
Chamomilla............................................cramps, leg aches
Crotalus horridus...............................jerking leg movement

Digitalis purpurea .............................heavy feeling in limbs
Lachesis mutus..........................cramps, sciatic discomforts
Lilium tigrinum....................................aching, restless legs
Pulsatilla ....................drawing pain in legs with restlessness
Rhus tox................................................muscular stiffness
Sulphur .................................burning sensation, heaviness
Tarentula hispana........................jerking, uneasiness in legs
Viscum album ..........................back, hip and leg discomfort
Zincum metallicum ....................jerking movements at night

** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″

† Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RESTLESS LEG SYMPTOM RELIEF 
arsenicum album, bufo rana, causticum, chamomilla, crotalus horridus, digitalis purpurea, lachesis mutus, lilium tigrinum, pulsatilla, rhus tox, sulphur, tarentula hispana, viscum album and zincum metallicum. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57955-9970
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	10 [hp_X]  in 59 mL
BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q)	BUFO BUFO CUTANEOUS GLAND	10 [hp_X]  in 59 mL
CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU)	CAUSTICUM	10 [hp_X]  in 59 mL
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ)	MATRICARIA CHAMOMILLA WHOLE	10 [hp_X]  in 59 mL
CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ956)	CROTALUS HORRIDUS HORRIDUS VENOM	10 [hp_X]  in 59 mL
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B)	DIGITALIS	10 [hp_X]  in 59 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	10 [hp_X]  in 59 mL
LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (LILIUM LANCIFOLIUM WHOLE FLOWERING - UNII:X67Z2963PI)	LILIUM LANCIFOLIUM WHOLE FLOWERING	10 [hp_X]  in 59 mL
PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	PULSATILLA VULGARIS WHOLE	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
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	10 [hp_X]  in 59 mL
LYCOSA TARANTULA (UNII: 86M454L2TT) (LYCOSA TARANTULA - UNII:86M454L2TT)	LYCOSA TARANTULA	10 [hp_X]  in 59 mL
VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP)	VISCUM ALBUM FRUITING TOP	10 [hp_X]  in 59 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	10 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57955-9970-2	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/13/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/13/2026

Labeler - King Bio Inc. (617901350)

Registrant - King Bio Inc. (617901350)

Establishment
Name	Address	ID/FEI	Business Operations
King Bio Inc.		617901350	manufacture(57955-9970) , api manufacture(57955-9970)