LUCKY BLUE ICE- menthol camphor gel

Lucky Blue Ice by

Drug Labeling and Warnings

Lucky Blue Ice by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Menthol 1.0%
Camphor 0.5%

Purpose

Topical Analgesic

Use

Lucky Super Soft Blue Ice Gel to provide temporary relief of minor pains and aches in your body's joints and muscles associated with:

• sports injuries
• sprains
• arthritis
• bruises
  

Warnings

for external use only
Do not apply to wound or damaged skin. Do not bandage the applied surface.
If condition worsens, discontinue use of this product.
Consult a physician if symptoms persist for more than 7 days.

Avoid contact with mucus membranes and eyes.

Do not use with heating devices or pads.

Keep out of reach of children

If pregnant or breast-feeding, ask a health professional before use

Directions

Apply liberally to painful zones and massage until absorbed into the skin. Repeat daily 3 or 4 times. Keep out of reach of children. Do not apply to children below two years of age.

Inactive Ingredients

Deionized Water, Isopropyl Alcohol, Propylene Glycol,Carbopol, PEG-40 Hydrogenated Castor Oil, Sodium Hydroxide,
Disodium EDTA, Benzyl Alcohol, BHT, FDC Blue No. 1

Package Label

INGREDIENTS AND APPEARANCE

LUCKY BLUE ICE 
menthol camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-210
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
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CARBOMER 934 (UNII: Z135WT9208)
EDETATE DISODIUM (UNII: 7FLD91C86K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-210-08	227 g in 1 JAR; Type 0: Not a Combination Product	11/15/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/15/2009

Labeler - Delta Brands Inc (102672008)