Label: DR. TALBOTS TUMMY ACHE RELIEF- calendula officinalis, carbo vegetabilis, chamomilla, foeniculum vulgare, lycopodium, nux moschata, zingiber officinale, kali muriaticum, magnesia phosphorica, natrum phosphoricum liquid
- NDC Code(s): 70797-311-01, 70797-311-04
- Packager: Talbot's Pharmaceuticals Family Products, LLC
- 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 October 5, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Pregnancy or breastfeeding
- Keep out of reach of children
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Directions
- Shake before use, natural juice may settle
- Measure only with the dosing syringe provided
- Do not use dosing syringe with other products
- On dosing syringe, weight is specific to product
- On dosing syringe, ml = milliliter, lbs = pounds, kgs = kilograms
Children under 6 months of age, consult a medical professional before using this product.
For sudden onset of symptoms: Use every 15 minutes for up to 8 doses until symptoms relieved, then every 2 hours thereafter.
Children 6 - 18 lbs or 3 - 8 kgs
1.25 ml every 2 hours, reduce frequency when symptoms improve
Children 19 - 29 lbs or 9 - 13 kgs
2.5 ml every 2 hours, reduce frequency when symptoms improve
Children 30 - 90 lbs or 14 - 41 kgs
5 ml every 2 hours, reduce frequency when symptoms improve
- Inactive Ingredients
- Questions
- Uses
- Warnings
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
DR. TALBOTS TUMMY ACHE RELIEF
calendula officinalis, carbo vegetabilis, chamomilla, foeniculum vulgare, lycopodium, nux moschata, zingiber officinale, kali muriaticum, magnesia phosphorica, natrum phosphoricum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70797-311 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 12 [hp_X] in 118 mL NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG 12 [hp_X] in 118 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_X] in 118 mL MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA CHAMOMILLA 12 [hp_X] in 118 mL CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 12 [hp_X] in 118 mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X] in 118 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 30 [hp_X] in 118 mL GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 12 [hp_X] in 118 mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X] in 118 mL FENNEL SEED (UNII: G3QC02NIE6) (FENNEL SEED - UNII:G3QC02NIE6) FENNEL SEED 12 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength APPLE JUICE (UNII: 9871T0PD5P) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70797-311-01 1 in 1 CARTON 07/10/2020 1 NDC:70797-311-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/10/2020 Labeler - Talbot's Pharmaceuticals Family Products, LLC (078855555)