IODIUM- iodium liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

Iodine (UNII: 9679TC07X4) (Iodine - UNII:9679TC07X4)

Available from:

Newton Laboratories, Inc.

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Fatigue, Thyroid problems, Goiter, Anxiety, Ravenous hunger.  Fatigue, Thyroid problems, Goiter, Anxiety, Ravenous hunger.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                IODIUM - IODIUM LIQUID
NEWTON LABORATORIES, INC.
_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._
----------
IODINE
INDICATIONS & USAGE SECTION
Fatigue, Thyroid problems, Goiter, Anxiety, Ravenous hunger.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give
3 drops) as needed or as
directed by a health professional. Sensitive persons begin with 1 drop
and gradually increase to full
dose.
OTC - ACTIVE INGREDIENT SECTION
Iodium 15x, 10x, 200c, 30c.
OTC - PURPOSE SECTION
Fatigue, Thyroid problems, Goiter, Anxiety, Ravenous hunger.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: USP Purified Water; USP Gluten-free, non-GMO,
organic cane alcohol 20%.
QUESTIONS SECTION
www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 -
Conyers, GA 30012
Questions? 1.800.448.7256
WARNINGS SECTION
WARNINGS: KEEP OUT OF REACH OF CHILDREN. DO NOT USE if tamper-evident
seal is broken or
missing. If symptoms worsen or persist for more than a few days,
consult a doctor. If PREGNANT OR
BREAST-FEEDING, ask a doctor before use.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If PREGNANT OR BREAST-FEEDING, ask a doctor before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
PACKAGE LABEL
Newton Laboratories, Inc.
IODIUM
iodium liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:55714-6 28 3
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
IO DINE (UNII: 9 6 79 TC0 7X4) (Io dine - UNII:9 6 79 TC0 7X4)
Io dine
15 [hp_X] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M)
WA TER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:55714-6 28 3-1
30 mL in 1 BOTTLE, GLASS
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R O
                                
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