NDC 70797-317

Dr Talbots Infant Tummy Ache Relief

Calendula Officinalis 12x,carbo Vegetabilis 12x,lycopodium 30x,foeniculum Vulgare 12x,nux Moschata 12x,zingiber Officinale 12x,kali Muriaticum 6x,magnesia Phosphorica 12x,natrum Phosphoricum 6x

Dr Talbots Infant Tummy Ache Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Talbot's Pharmaceuticals Family Products,llc.. The primary component is Activated Charcoal; Calendula Officinalis Flowering Top; Fennel Seed; Ginger; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Chamomilla; Nutmeg; Potassium Chloride; Sodium Phosphate, Dibasic, Heptahydrate.

• Product ID: 70797-317_e9c24994-b936-36e6-e053-2a95a90a78df
• NDC: 70797-317
• Product Type: Human Otc Drug
• Proprietary Name: Dr Talbots Infant Tummy Ache Relief
• Generic Name: Calendula Officinalis 12x,carbo Vegetabilis 12x,lycopodium 30x,foeniculum Vulgare 12x,nux Moschata 12x,zingiber Officinale 12x,kali Muriaticum 6x,magnesia Phosphorica 12x,natrum Phosphoricum 6x
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2022-09-28
• Marketing Category: UNAPPROVED HOMEOPATHIC /
• Labeler Name: Talbot's Pharmaceuticals Family Products,LLC.
• Substance Name: ACTIVATED CHARCOAL; CALENDULA OFFICINALIS FLOWERING TOP; FENNEL SEED; GINGER; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA CHAMOMILLA; NUTMEG; POTASSIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
• Active Ingredient Strength: 12 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL
• Pharm Classes: Allergens [CS], Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Plant Proteins [CS], Plant Proteins [CS], Potassium Compounds [CS], Potassium Salt [EPC], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 70797-317-01

1 BOTTLE in 1 CARTON (70797-317-01) > 118 mL in 1 BOTTLE

• Marketing Start Date: 2022-09-28
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details