UDDER ESSENCE BETTER BALM MEDICATED- menthol and methyl salicylate cream

Udder Essence Better Balm Medicated by

Drug Labeling and Warnings

Udder Essence Better Balm Medicated by is a Animal medication manufactured, distributed, or labeled by LC&G Distributing Inc., Dynamic Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Medicated Better Balm is a topical aid for irritation from minor cuts, scrapes, scratches, and chapping.

WARNINGS

KEEP OUT OF REACH OF CHILDREN

Avoid contact with eyes.

For External use only.

Discontinue use if irritation occurs.

Not to be applied to deep or puncture wounds.

Directions

Apply liberally to clean exposed areas. Repeat as necessary.

Ingredients

Water, Mineral Oil, Glycerin, Cetearyl Alcohol, Stearic Acid, Propylene Glycol, Sorbitol, Glycol Stearate, Potassium Hydroxide, Lanolin, Methyl Paraben, Propyl Paraben, Menthol, Methyl Salicylate, Tocopherol Acetate (Vitamin E), Aloe Vera Gel, Retinyl Palmitate (Vitamin A), Cholecalciferol (Vitamin D), FD&C Blue #1.

Questions or Comments?

PO Box 6874, Spring Hill, FL 34611

PRINCIPAL DISPLAY PANEL - 454 Gram Jar

Vitamins
A, D and E
Aloe Vera Gel
Lanolin

Udder Essence

BETTER BALM
Medicated

Net Weight
16oz. (1LB.)
(454 grams)

INGREDIENTS AND APPEARANCE

UDDER ESSENCE BETTER BALM MEDICATED 
menthol and methyl salicylate cream

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 24465-879
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A)	Menthol	0.25 g  in 100 g
Methyl Salicylate (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Methyl Salicylate	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Mineral Oil (UNII: T5L8T28FGP)
Glycerin (UNII: PDC6A3C0OX)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Stearic Acid (UNII: 4ELV7Z65AP)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitol (UNII: 506T60A25R)
Glycol Stearate (UNII: 0324G66D0E)
Potassium Hydroxide (UNII: WZH3C48M4T)
Lanolin (UNII: 7EV65EAW6H)
Methylparaben Sodium (UNII: CR6K9C2NHK)
Propylparaben Sodium (UNII: 625NNB0G9N)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Vitamin A (UNII: 81G40H8B0T)
Cholecalciferol (UNII: 1C6V77QF41)
FD&C Blue No. 1 (UNII: H3R47K3TBD)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24465-879-16	454 g in 1 JAR
2	NDC: 24465-879-03	85 g in 1 TUBE
3	NDC: 24465-879-04	1816 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved Drug Other		03/01/2011

Labeler - LC&G Distributing Inc. (795315436)

Establishment
Name	Address	ID/FEI	Business Operations
Dynamic Pharmaceuticals Inc.		617660712	MANUFACTURE, API MANUFACTURE