Label: DR TALBOTS INFANT MUCUS COLD RELIEF- eupatorium perf 12x,hepar sulphuris calcareum 12x,kali bichromicum 12x,marrubium vulgare 12x,phosphorus 30x,pulsatilla 12x,rumex crispus 12x,sambucus nigra 12x,calcarea sulphurica 12x,ferrum phosphoricum 12x liquid
- NDC Code(s): 70797-320-01
- 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 September 13, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PREGNACY
- ASK A DOCTOR
- INACTIVE INGREDIENTS
- QUESTIONS
-
Warnings
Warnings:
Do not use:
- for persistent or chronic cough
- for treating cough from asthma, smoking, or emphysema
- for treating cough with excessive mucus.
A persistent may be a sign of a serious condition.
Stop use and ask doctor if:
- cough/congestion lasts for more than 7 days.
- cough/congestion comes back, or is accompanied by fever, rash, or persistent headache. these could be signs of a serious condition.
- other symptoms persist for more than 7 days or worsen.
-
Dosage
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, every 2 hours thereafter.Children Dose
6 - 18 lbs or 3 - 8 kgs 1.25 mL every 2 hours*
19 - 29 lbs or 9 - 13 kgs 2.5 mL every 2 hours*
30 - 90 lbs or 14 - 41 kgs 5 mL every 2 hours*
*Reduce frequency when symptoms improve. - Keep out of reach of children
- Uses
- Purpose
- PRICIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR TALBOTS INFANT MUCUS COLD RELIEF
eupatorium perf 12x,hepar sulphuris calcareum 12x,kali bichromicum 12x,marrubium vulgare 12x,phosphorus 30x,pulsatilla 12x,rumex crispus 12x,sambucus nigra 12x,calcarea sulphurica 12x,ferrum phosphoricum 12x liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70797-320 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (MARRUBIUM VULGARE - UNII:7A72MUN24Z) MARRUBIUM VULGARE 12 [hp_Q] in 118 mL SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (SAMBUCUS NIGRA FLOWERING TOP - UNII:CT03BSA18U) SAMBUCUS NIGRA FLOWERING TOP 12 [hp_X] in 118 mL CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE ANHYDROUS 12 [hp_X] in 118 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_X] in 118 mL EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP 12 [hp_X] in 118 mL ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA 12 [hp_X] in 118 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 12 [hp_X] in 118 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 118 mL FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 12 [hp_X] in 118 mL RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT 12 [hp_X] in 118 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_X] in 118 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CONCORD GRAPE JUICE (UNII: F7039Q79LP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70797-320-01 1 in 1 CARTON 09/12/2022 1 118 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 09/12/2022 Labeler - Talbot’s Pharmaceuticals Family Products, LLC. (078855555)