Label: CORONA MULTI-PURPOSE- lanolin ointment
- NDC Code(s): 86077-0030-1, 86077-0030-2, 86077-0030-3, 86077-0030-4
- Packager: Manna Pro Products LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 14, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INFORMATION FOR PATIENTS
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
For Minor Cuts, Sores, Burns, Chapping, Dry Skin
SINCE 1906
CORONA
MULTI-PURPOSE OINTMENT
Helps Promote Healing
Soothes Irritated Skin
Prevents Drying & Cracking
Creates a Barrier Againts Insects, Moisture & Dirt
No Gloves Needed To Apply
CORONA MULTIPURPOSE OINTMENT
For over 100 years, Corona Ointment has been protecting skin and helping to promote the natural healing of minor cuts, sores, burns, chapping, and dry skin. The lanolin-based formula helps to soothe irritated skin and prevents drying & cracking. The thick ointment creates a barrier against insects, moisture, and dirt, plus it stays in place giving the irritated area long-lasting protection. It is non-toxic and does not require gloves to be applied. Corona Ointment works so well that no barn should be without it!
Manna Pro Products, LLC
707 Spirit 40 Park Dr.
Suite 150
St. Louis, MO 63005
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INGREDIENTS AND APPEARANCE
CORONA MULTI-PURPOSE
lanolin ointmentProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86077-0030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 30 g in 100 g Inactive Ingredients Ingredient Name Strength DMDM HYDANTOIN (UNII: BYR0546TOW) YELLOW WAX (UNII: 2ZA36H0S2V) EDETATE DISODIUM (UNII: 7FLD91C86K) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) METHYL SALICYLATE (UNII: LAV5U5022Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86077-0030-1 56.7 g in 1 JAR 2 NDC:86077-0030-3 396.9 g in 1 JAR 3 NDC:86077-0030-4 1020.6 g in 1 JAR 4 NDC:86077-0030-2 198.45 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2017 Labeler - Manna Pro Products LLC (147666812)