Medic Ice by Straight Arrow Products, Inc. MEDIC ICE- menthol gel

Medic Ice by

Drug Labeling and Warnings

Medic Ice by is a Otc medication manufactured, distributed, or labeled by Straight Arrow Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Menthol 7%

PURPOSE

Purpose

Pain relieving gel

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.

INDICATIONS & USAGE

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

WARNINGS

• For external use only

Do not use

•  on wounds or damaged skin
• with heating pads or heating devices
•  with other ointments, creams, sprays or liniments
•  with tight bandages

When using this product

• avoid contact with eyes
  

Stop use and ask a doctor if:

• a rash appears
• condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days
  

If pregnant or breast-feeding, ask a doctor before use.

DOSAGE & ADMINISTRATION

Directions

• Adults and children 2 years and over: Clean skin of all other ointments, creams, sprays or liniments.  Apply directly to affected areas no more than 3 to 4 times daily.  Wash hands after application to help avoid contact with eyes and sensitive areas. May be used with wet or dry bandages or with ice packs.
• Children under 2 years of age:  ask a doctor

INACTIVE INGREDIENT

Inactive Ingredients   Water, Alcohol, Laureth-4, Carbomer, Triethanolamine, Aloe Vera, Benzocaine, Thymol, Camphor, Methylsulfonylmethane (MSM), Glucosamine HCl, Chondroitin Sulfate, Oil Complex - (Oregano, Eucalyptus, Sage, Patchouli, Lavender, Rosemary, Ginger, Peppermint), Fragrance, Mineral Complex - (Magnesium Sulfate, Copper Sulfate, Calcium Sulfate, Calcium Carbonate, Lithium Chloride, Potassium Chloride, Sodium Sesquicarbonate, Ammonium Chloride), Herbal Complex - (Arnica, Slippery Elm, Chickweed, Comfrey, Myrrh, Hops, Marshmallow, Plantain, Green Tea), FD and C Blue No. 1.

PRINCIPAL DISPLAY PANEL

ID:                        Med1
Descriptive Text:   Medic Ice label
File Name:            medicice.jpg

INGREDIENTS AND APPEARANCE

MEDIC ICE  
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62001-0318
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	.07 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
BENZOCAINE (UNII: U3RSY48JW5)
LAURETH-4 (UNII: 6HQ855798J)
THYMOL (UNII: 3J50XA376E)
ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
ALOE (UNII: V5VD430YW9)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
PEPPERMINT OIL (UNII: AV092KU4JH)
EUCALYPTUS OIL (UNII: 2R04ONI662)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
ROSEMARY OIL (UNII: 8LGU7VM393)
PATCHOULI OIL (UNII: F3IN55X5PO)
GINGER OIL (UNII: SAS9Z1SVUK)
SAGE OIL (UNII: U27K0H1H2O)
OREGANO (UNII: 0E5AT8T16U)
GLUCOSAMINE (UNII: N08U5BOQ1K)
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
LITHIUM CHLORIDE (UNII: G4962QA067)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
CUPRIC SULFATE ANHYDROUS (UNII: KUW2Q3U1VV)
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
CALCIUM SULFATE (UNII: WAT0DDB505)
CALCIUM CARBONATE (UNII: H0G9379FGK)
ARNICA MONTANA (UNII: O80TY208ZW)
ELM (UNII: 63POE2M46Y)
STELLARIA MEDIA (UNII: 2H03479QVR)
COMFREY (UNII: D05HXK6R3G)
MYRRH (UNII: JC71GJ1F3L)
HOPS (UNII: 01G73H6H83)
PLANTAGO MAJOR (UNII: W2469WNO6U)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62001-0318-1	318880.8 g in 1 CONTAINER
2	NDC: 62001-0318-2	454 g in 1 CONTAINER
3	NDC: 62001-0318-3	71 g in 1 TUBE, WITH APPLICATOR
4	NDC: 62001-0318-4	113 g in 1 TUBE
5	NDC: 62001-0318-5	4 g in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/24/2004

Labeler - Straight Arrow Products, Inc. (061580593)

Registrant - Straight Arrow Products, Inc. (061580593)

Establishment
Name	Address	ID/FEI	Business Operations
Straight Arrow Products, Inc.		061580593	manufacture