Morning Sickness description, usages, side effects, indications, overdosage, supplying and lots more!

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Morning Sickness

Newton Laboratories, Inc.
Newton Laboratories, Inc.

Morning Sickness


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

INDICATIONS & USAGE SECTION

Morning Sickness  Formulated for associated symptoms such as dizziness, discomfort, indigestion, nausea, vomiting and loss of appetite.

DOSAGE & ADMINISTRATION SECTION

Directions: ORAL USE ONLY - SHAKE WELL.  Adults, take 6 drops orally as needed or as directed by a healthcare professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Bismuthum metallicum 15x, Bryonia 15x, Cimicifuga 15x, Gossypium herbaceum 15x, Ipecac. 15x, Kreosotum 15x, Lycopodium 15x, Mag. carb. 15x, Nux vom. 15x, Pulsatilla 15x, Sepia 15x, Symphoricarpus racemosus 15x, Tabacum 15x, Zingiber 15x, Chamomilla 3x, Hydrastis 3x, Iris versicolor 3x.

OTC - PURPOSE SECTION

Formulated for associated symptoms such as dizziness, discomfort, indigestion, nausea, vomiting and loss of appetite.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.  

QUESTIONS SECTION

www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions?  1.800.448.7256 

WARNINGS SECTION

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

Morning Sickness

Bismuthum metallicum, Bryonia, Cimicifuga, Gossypium herbaceum, Ipecac., Kreosotum, Lycopodium, Mag. carb., Nux vom., Pulsatilla, Sepia, Symphoricarpus racemosus, Tabacum, Zingiber, Chamomilla, Hydrastis, Iris versicolor LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55714-2322
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Bismuth Bismuth 15 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 15 [hp_X]
BLACK COHOSH BLACK COHOSH 15 [hp_X]
GOSSYPIUM HERBACEUM ROOT BARK Gossypium Herbaceum Root Bark 15 [hp_X]
Ipecac IPECAC 15 [hp_X]
WOOD CREOSOTE WOOD CREOSOTE 15 [hp_X]
Lycopodium Clavatum Spore LYCOPODIUM CLAVATUM SPORE 15 [hp_X]
MAGNESIUM CARBONATE 15 [hp_X]
STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED 15 [hp_X]
PULSATILLA VULGARIS PULSATILLA VULGARIS 15 [hp_X]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE 15 [hp_X]
Symphoricarpos Albus Fruit Symphoricarpos Albus Fruit 15 [hp_X]
TOBACCO LEAF TOBACCO LEAF 15 [hp_X]
GINGER 15 [hp_X]
Matricaria Recutita MATRICARIA RECUTITA 3 [hp_X]
GOLDENSEAL GOLDENSEAL 3 [hp_X]
Iris Versicolor Root Iris Versicolor Root 3 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55714-2322-1 29.57 in 1 BOTTLE, GLASS
2 NDC:55714-2322-2 59.14 in 1 BOTTLE, GLASS
3 NDC:55714-2322-0 .5 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-03-01


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