Pleo Spermus description, usages, side effects, indications, overdosage, supplying and lots more!

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Pleo Spermus

Sanum Kehlbeck GmbH & Co. KG

Pleo™ Spermus DROPS 1X


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Homeopathic Medicine

1 fl oz
(30 mL)

Indications

For relief of diarrhea and stomach upset.

INGREDIENTS

30 mL contains: Leptospermum scoparium 1X in a base of purified water, ethanol (70%).

Tamper Evident

Use this product only if tamper-evident strip on base of bottle cap is intact.

DOSAGE

Take 5 drops, 1–3 times daily, unless otherwise recommended by your health care professional.

WARNING

If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.

Keep this and all medications out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Protect from light and heat.

Made in Germany.

Distributed by:
SANUM USA Corp.
1465 Slater Road
Ferndale, WA 98248

Manufactured By:
Sanum-Kehlbeck,
GmbH & Co. KG

Rev. 08/2000

PRINCIPAL DISPLAY PANEL - 30 mL Label

Pleo™ Spermus DROPS 1X

Homeopathic Medicine

Indications: For relief of diarrhea and stomach upset.

1 fl oz (30 mL)

DOSAGE: Take 5 drops 1-3 times daily; unless otherwise recommended by your health care
professional. WARNING: If symptoms persist, contact a licensed practitioner. If pregnant or
nursing, seek advice of a health care professional before use. Keep this and all medications
out of the reach of children.
In case of accidental overdose, seek professional assistance or
contact a Poison Control Center immediately. Protect from light and heat. TAMPER EVIDENT:
Do not use this product if tamper-evident seal on base of bottle cap is missing or broken.
INGREDIENTS: 30 mL contains: Leptospermum scoparium 1X in a base of purified water,
ethanol (70 %).
Rev. 06/2009

Pleo Spermus

Pleo Spermus

Manuka Oil SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60681-1311
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MANUKA OIL 1 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, DROPPER
2 NDC:60681-1311-3 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2006-01-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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