Apeaz Ultra description, usages, side effects, indications, overdosage, supplying and lots more!

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Apeaz Ultra

Innovus Pharmaceuticals, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Camphor 4%

Menthol 10%

Methyl Salicylate 30%

Purpose

topical analgesic

Apeaz Ultra Uses

Temporarily relieves the minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises sprains

Warnings

For external use only

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age
  • with arthritis like conditions

Ask a doctor before use

If you have redness over the affected area

When using this product

Avoid contact with eyes or mucus membranes
Do not bandage tightly

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or symptoms clear up and occur again within a few days
  • excessive skin irritation occurs

Keep out of the reach of children to acoid accidental ingestion

If swallowed, get medical help or contact a Poison Center immediately

Directions

Use only as directed

Adults and children 12 years of age and older, apply to affected area not more than 3 to 4 times daily

Children under 12 years of age: ask a doctor

Inactive Ingredients

Lanolin USP, Ethyl & propylparabens, Polysorbate 80, PEG-100 Stearate, Petrolatum, Deionized Water, Carbopol 940, DMDM hydantion, EDTA glycol mono stearate, Stearic acid FLK triple press

Other information

Store at 20-25 (68-77F)

Questions

858-964-5123

Apeaz Ultra

Apeaz Ultra

camphor, menthol, methyl salicylate cream CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57483-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (SYNTHETIC) 40 mg
MENTHOL 100 mg
methyl salicylate METHYL SALICYLATE 300 mg

Inactive Ingredients

Ingredient Name Strength
METHYLPARABEN
PROPYLPARABEN
polysorbate 80
PEG-100 STEARATE
petrolatum
water
CARBOMER HOMOPOLYMER TYPE C
DMDM HYDANTOIN
EDETIC ACID
GLYCOL STEARATE
STEARIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57483-001-04 56.7 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-08-06


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Be sure to consult your doctor before taking any medication!
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