LIP RECOVERY- petrolatum ointment

LIP RECOVERY by

Drug Labeling and Warnings

LIP RECOVERY by is a Otc medication manufactured, distributed, or labeled by PHARMAGEL INTERNATIONAL INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

PETROLATUM............................48%

PURPOSE

LIP PROTECTANT

USES

HELPS PROTECT, RELIEVE, AND PREVENT CHAPPED LIPS
HELPS PROTECT FROM THE DRYING EFFECTS OF WIND AND COLD WEATHER

WARNINGS

WHEN USING THIS PRODUCT

• DO NOT GET INTO EYES.
• AVOID CONTACT WITH THE EYES. IF PRODUCT GETS INTO THE EYES, RINSE THOROUGHLY WITH WATER.

STOP USE AND ASK DOCTOR

IF IRRITATION OR RASH DEFELOPS AND CONTINUES FOR MORE THAN 72 HOURS.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions:

Apply daily to lips. Reapply as needed.

INACTIVE INGREDIENTS:

HYDROGENATED POLYISOBUTENE, TRIACONTANYL PVP, BUTYROSPERMUM PARKII BUTTER, PARAFFIN, SILICA, ETHYLENE/PROPYLENE/STYRENE COPOLYMER, ISOHEXA- DECANE, CYCLOPENTASILOXANE, TOCOPHEROL, SODIUM HYALURONATE, TRIPEPTIDE-1, TETRAHEXYLDECYL ASCOR- BATE, RETINYL PALMITATE, TOCOPHERYL ACETATE, ALOE BARBADENSIS (ALOE VERA) LEAF EXTRACT, COCOS NUCIFERA (COCONUT) OIL, DIMETHYLAMINOETHANOL TARTRATE, ETHYLHEXYL METHOXYCINNAMATE, BENZO- PHENONE-3, BUTYLENE/ETHYLENE/STYRENE COPOLYMER, BIS-PEG/PPG-14/14 DIMETHICONE, XANTHAN GUM, BHT, BENZYL ALCOHOL,PHENOXYETHANOL

Questions or Comments?

Call 800.882.1889

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIP RECOVERY 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67879-307
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	48 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
SHEA BUTTER (UNII: K49155WL9Y)
PARAFFIN (UNII: I9O0E3H2ZE)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLENE (UNII: 91GW059KN7)
PROPYLENE (UNII: AUG1H506LY)
STYRENE (UNII: 44LJ2U959V)
ISOHEXADECANE (UNII: 918X1OUF1E)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TOCOPHEROL (UNII: R0ZB2556P8)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PREZATIDE (UNII: 39TG2H631E)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
COCONUT OIL (UNII: Q9L0O73W7L)
DEANOL BITARTRATE (UNII: D240J05W14)
OCTINOXATE (UNII: 4Y5P7MUD51)
OXYBENZONE (UNII: 95OOS7VE0Y)
1-BUTENE (UNII: LY001N554L)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67879-307-51	1 in 1 BOX	06/13/2016
1	NDC: 67879-307-11	15 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/18/2015

Labeler - PHARMAGEL INTERNATIONAL INC (603215182)

Registrant - PHARMAGEL INTERNATIONAL INC (603215182)