OSTEODORON PM SPECIAL FORMULA powder

Country: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Virkt innihaldsefni:

CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4), LEAD CARBONATE (UNII: 43M0P24L2B) (LEAD - UNII:2P299V784P), OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z), QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W)

Fáanlegur frá:

Uriel Pharmacy Inc.

Stjórnsýsluleið:

ORAL

Gerð lyfseðils:

OTC DRUG

Ábendingar:

Directions: FOR ORAL USE ONLY. Uses: For healthy bone and teeth development.

Leyfisstaða:

unapproved homeopathic

Vara einkenni

OSTEODORON PM SPECIAL FORMULA- OSTEODORON PM SPECIAL
FORMULA POWDER
URIEL PHARMACY 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._
----------
OSTEODORON PM SPECIAL FORMULA
Directions: FOR ORAL USE ONLY.
Take in the evening. Use in combination with Osteodoron AM Special
Formula Powder.
Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age
2: Consult a
doctor.
Active Ingredients: 100 gm contains: 5 gm Conchae (Oyster shell) 1X;
Quercus (Oak
bark) 4X, Fluorite (Calcium fluoride) 6X, Quartz (Rock crystal) 6X,
Cerussite (White lead
ore) 8X
Inactive Ingredient: Lactose
Uses: For healthy bone and teeth development.
KEEP OUT OF REACH OF CHILDREN.
Warnings: Claims based on traditional homeopathic practice, not
accepted medical
evidence. Not FDA evaluated. Do not use if allergic to any ingredient.
Contains lactose.
Consult a doctor before use for serious conditions or if conditions
worsen or persist. If
pregnant or nursing, consult a doctor before use. Do not use if safety
seal is broken or
missing.
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com
OSTEODORON PM SPECIAL FORMULA
osteodoron pm special formula powder
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-7161
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)
CALCIUM FLUORIDE
6 [hp_X]
in 1 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
SILICON DIOXIDE
6 [hp_X]
in 1 g
LEAD CARBONATE (UNII: 43M0P24L2B) (LEAD - UNII:2P299V784P)
LEAD CARBONATE
8 [hp_X]
in 1 g
OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL -
UNII:49OY13BE7Z )
OSTREA EDULIS
SHELL
1 [hp_X]
in 1 g
QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE -
UNII:R7QMG0BT2W)
QUERCUS ROBUR
WHOLE
4 [hp_X]
in 1 g