FOOT PAIN RELIEVING- apis mellifica, gelsemium sempervirens, gnaphalium spray 
The Magni Group Inc

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.

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Active Ingredients (In Spray) - Purpose
Apis Mellifica 3X HPUS - Relieves Foot Pain
Gnaphalium 3X HPUS - Relieves Foot Pain
Gelsemium Sempervirens 6X HPUS - External Analgesic

Pain Relieving Foot Spray

NDC: 43689-0040

Purpose:
Relieves Foot Pain
External Analgesic

NDC: 43689-0040

Use:
Temporarily relieves foot pain

NDC: 43689-0040

Keep out of reach of children

NDC:

Warning:
For external use only

NDC: 43689-0040

When using this product:
- Avoid contact with eyes

NDC: 43689-0040

If symptoms persist for more than 7 days or worsen,
consult your physician

NDC: 43689-0040

Do not use on open wounds, cuts, damaged, or infected skin

NDC: 43689-0040

Directions:
- Adults and children 12 years of age and older, apply to all surfaces of the feet, heels and toes up to four times daily
- Apply to legs as needed

NDC: 43689-0040

Other information:
- Most beneficial when applied after bathing, showering, or a foot soak
- The letter "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States
- These statements are supported by the traditional homeopathic principles

NDC: 43689-0040

Inactive Ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzoic Acid, Bergamot Oil, C14-22 Alcohol/C12-20 Alkyl Glucoside, Canola Oil, Camphor Gum, Citric Acid, Ethylhexyl Stearate, Eucalyptus Oil, Glycerin, Mentha Piperita (Peppermint) Extract, Menthol, Methyl Salicylate, Panthenol, Phenoxyethanol, Sodium Hydroxide, Sorbic Acid, Tocopheryl Acetate, Water (Aqua), Xanthan Gum

NDC: 43689-0040

Principal Display Panel

Principal Display Panel

NDC: 43689-0040

FOOT PAIN RELIEVING 
apis mellifica, gelsemium sempervirens, gnaphalium spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA3 [hp_X]  in 100 g
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]  in 100 g
PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57) (PSEUDOGNAPHALIUM LUTEOALBUM LEAF - UNII:BGI20Z6M57) PSEUDOGNAPHALIUM LUTEOALBUM LEAF3 [hp_X]  in 100 g
Inactive Ingredients
Ingredient NameStrength
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SORBIC ACID (UNII: X045WJ989B)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
C14-22 ALCOHOLS (UNII: B1K89384RJ)  
CANOLA OIL (UNII: 331KBJ17RK)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9)  
BERGAMOT OIL (UNII: 39W1PKE3JI)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PANTHENOL (UNII: WV9CM0O67Z)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43689-0040-185 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic12/29/2020
Labeler - The Magni Group Inc (113501902)
Establishment
NameAddressID/FEIBusiness Operations
United Laboratories Manufacturing LLC807878116manufacture(43689-0040)

Revised: 12/2020
Document Id: b072c546-7807-52cb-e053-2a95a90ab1b4
Set id: b072c546-7806-52cb-e053-2a95a90ab1b4
Version: 1
Effective Time: 20201229
 
The Magni Group Inc