DT ICE COLD ANALGESIC- menthol gel

DT Ice Cold Analgesic by

Drug Labeling and Warnings

DT Ice Cold Analgesic by is a Otc medication manufactured, distributed, or labeled by Volume Distributors, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS

Active ingredients                        Purpose

Menthol (1%)................................Topical Analgesic

PURPOSE

Purpose
topical analgesic

INDICATIONS & USAGE

Uses-

temporarily relieves:minor muscle aches and pains

WARNINGS

Warnings

For external use only; avoid contact with eyes.

ASK DOCTOR

Ask a doctor before use if you have cough associated with
smoking
excessive phlegm
asthma
emphysema
persistent or chronic cough

WHEN USING

When using this product

Do not heat
microwave
add to hot water or any container where healing water may cause splattering and result in burns
use in eyes or directly on mucous membranes
take by mouth or place in nostrils
apply to wounds or damaged skin.
bandage skin.

STOP USE

Consult a doctor and discontinue use;
if condition worsens, persists for more than 1 week or tends to recur.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION

Directions

For the temporary relief of minor muscle aches and pains.
See important warnings under "When Using This Product"

not for use on children under 2 years of age
adults and children 2 y ears and older: apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

INACTIVE INGREDIENT

Inactive Ingredients: Camphor, Carbomer, FDandC Blue No1, Isopropyl Alcohol, methylchloroisothiazolinone, methylisothiazolinone, Sodium hydroxide, water.

PRINCIPAL DISPLAY PANEL

DT ICE COLD
ANALGSIC GEL

Distributed by:
DT products
Vernon,CA 90058
MADE IN CHINA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DT ICE COLD ANALGESIC 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50523-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50523-000-08	227 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	12/22/2010

Labeler - Volume Distributors, Inc. (002029544)