Ocean Potion Instant Burn Relief Ice description, usages, side effects, indications, overdosage, supplying and lots more!

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Ocean Potion Instant Burn Relief Ice

Sun & Skin Care Research, LLC

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Lidocaine 0.5%

Purpose

Temporarily Relieves pain due to:

  • sunburn
  • minor burns

Ocean Potion Instant Burn Relief Ice Uses

Temporarily Relieves pain and itching due to:

  • sunburn
  • minor burns

Warnings

For external use only.  Do not swallow.  Avoid contact with eyes.  If contacted, flush eyes with water.  Should a rash or irritation develops, discontinue use.  If condition worsens, or if symptoms persist for more than 7 days, consult a physician.  Do not use in large quantities, particularly over raw surfaces or blistered areas.  Keep out of the reach of children.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Acrylates / C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, CI 42090, DMDM Hydantoin, Fragrance, Glycerin, Isoceteth-20, Melaleuca Alternifolia (Tea Tree Oil), Menthol, Methylparaben, Phenoxyethanol, Propylene Glycol, Propylparaben, Symphytum Officinale (Comfrey) Extract, Triethanolamine, Water

Directions

Adults and children 2 years of age and older, apply to the affected area not more than 3 to 4 times daily.  Children under 2 years of age, consult a physician.


  • protect this product from excessive heat and direct sun
  • for use on skin only

Ocean Potion Instant Burn Relief Ice

Ocean Potion Instant Burn Relief Ice

lidocaine GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62802-172
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE LIDOCAINE .5 g

Inactive Ingredients

Ingredient Name Strength
water
isoceteth-20
propylene glycol
Aloe Vera Leaf
GLYCERIN
MENTHOL
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
DMDM HYDANTOIN
PHENOXYETHANOL
METHYLPARABEN
PROPYLPARABEN
TROLAMINE
ARNICA MONTANA FLOWER
COMFREY LEAF
TEA TREE OIL
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62802-172-65 605 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-01-01


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Be sure to consult your doctor before taking any medication!
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