DB FOOT PAIN RELIEVING- apis mellifica, gelsemium sempervirens, gnaphalium spray
DB Foot Pain Relieving by
Drug Labeling and Warnings
DB Foot Pain Relieving by is a Homeopathic medication manufactured, distributed, or labeled by The Magni Group Inc, United Laboratories Manufacturing LLC. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Active Ingredients (In Spray) - Purpose Apis Mellifica 3X HPUS - Relieves Foot Pain Gnaphalium 3X HPUS - Relieves Foot Pain Gelsemium Sempervirens 6X HPUS - External Analgesic
- Purpose: Relieves Foot Pain External Analgesic
- Use: Temporarily Relieves Foot Pain
- Keep out of reach of children
- Warnings: For external use only
- When using this product: - Avoid contact with eyes
- If symptoms persist for more than 7 days or worsen, consult your physician
- Do not use on open wounds, cuts, damaged, or infected skin
- Directions: - Adults and children 12 years of age and older, apply to all surfaces on the feet, heels and toes up to four times daily - Apply to legs as needed
- Other information: - Most beneficial when applied after bathing, showering, or a foot soak - The letters "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
- 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
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
DB FOOT PAIN RELIEVING
apis mellifica, gelsemium sempervirens, gnaphalium sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 43689-0039 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57) (PSEUDOGNAPHALIUM LUTEOALBUM LEAF - UNII:BGI20Z6M57) PSEUDOGNAPHALIUM LUTEOALBUM LEAF 3 [hp_X] in 100 g APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 3 [hp_X] in 100 g GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X] in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) CANOLA OIL (UNII: 331KBJ17RK) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) METHYL SALICYLATE (UNII: LAV5U5022Y) SORBIC ACID (UNII: X045WJ989B) MENTHOL (UNII: L7T10EIP3A) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) C14-22 ALCOHOLS (UNII: B1K89384RJ) MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9) BERGAMOT OIL (UNII: 39W1PKE3JI) GLYCERIN (UNII: PDC6A3C0OX) EUCALYPTUS OIL (UNII: 2R04ONI662) XANTHAN GUM (UNII: TTV12P4NEE) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BENZOIC ACID (UNII: 8SKN0B0MIM) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 43689-0039-1 85 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/29/2020 Labeler - The Magni Group Inc (113501902) Establishment Name Address ID/FEI Business Operations United Laboratories Manufacturing LLC 807878116 manufacture(43689-0039)
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.