BLISTEX LIP OINTMENT

Active Ingredients:

Dimethicone 1.1% (w/w)

Camphor 0.5% (w/w)

Menthol 0.6% (w/w)

Phenol 0.5% (w/w)

Purpose:

Skin protectant

External analgesic

Uses: for the temporary protection and relief of pain and itching associated with

minor lip irritation
chapped or cracked lips
cold sores

Warnings: For external use only

Do not use

in the eyes or over large portions of the body
on deep or puncture wounds
on animal bites
on serious burns

Stop use and ask a doctor if

condition worsens
condition lasts for more than 7 days
symptoms clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

Directions

Adults and children 2 years of age and over: apply liberally to affected area not more than 3 to 4 times daily

Children under 2 years of age: ask a doctor

Inactive Ingredients: Allontoin, Ammonium Hydroxide, Beeswax, Calcium Disodium EDTA, Calcium Hydroxide, Cetyl Alcohol, Flavors, Glycerin, Lanolin, Lauric Acid, Mineral Oil, Myristic Acid, Oleic Acid, Palmitic Acid, Paraffin, Petrolatum, Polyglyceryl-3 diisostearate, Potassium Hydroxide, Purified Water, SD Alcohol 36, Silica, Sodium Hydroxide, Sodium Saccharin, Stearyl Alcohol

BLISTEX LIP
dimethicone, camphor, menthol, phenol ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50332-0028
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	1.1 g in 100 g
CAMPHOR OIL (UNII: 75IZZ8Y727) (CAMPHOR OIL - UNII:75IZZ8Y727)	CAMPHOR OIL	.5 g in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	.6 g in 100 g
PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV)	PHENOL	.5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALLANTOIN (UNII: 344S277G0Z)
EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)
CALCIUM HYDROXIDE (UNII: PF5DZW74VN)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)
LANOLIN (UNII: 7EV65EAW6H)
LAURIC ACID (UNII: 1160N9NU9U)
MINERAL OIL (UNII: T5L8T28FGP)
MYRISTIC ACID (UNII: 0I3V7S25AW)
OLEIC ACID (UNII: 2UMI9U37CP)
PALMITIC ACID (UNII: 2V16EO95H1)
PARAFFIN (UNII: I9O0E3H2ZE)
PETROLATUM (UNII: 4T6H12BN9U)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:50332-0028-2	25 in 1 BOX, UNIT-DOSE	08/09/1995
1		.5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M	08/09/1995

Labeler - HART Health (069560969)

Registrant - HART Health (069560969)