UDDER BALM: Product Information

UDDER BALM — oxyquinoline ointment
H. W. Naylor Company Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Label

Active Ingredients

8-Hydroxyquinoline .14%

Purpose

Chapped teats, Minor cuts, scrapes, scratches, chafes, windburn, sunburn.

Directions

Apply liberally after each milking or as often as necessary.

Safety

CAUTION: Do not use in case of deep puncture wounds or serious burns – consult veterinarian.

If redness, irritation or swelling persists or increases, discontinue use and consult veterinarian.

Thoroughly wash udder and teats before milking.

Animal Use Only

KEEP FROM REACH OF CHILDREN

Other Ingredients

Petrolatum, Water, Lanolin, Wax, Oil of Clove, Sodium Borate, Color, Isopropyl Alcohol .2%.

Questions?

H. W. NAYLOR CO., INC.
MORRIS, NY 13808 U.S.A.

Principal Display Panel

Dr. Naylor®
UDDER BALM
NET WT. 9 OZ. (255 GRAMS)

H.W. NAYLOR CO., INC.
MORRIS, NY 13808 U.S.A.
ANTISEPTIC OINTMENT FOR UDDER AND TEATS
Designed to remain in prolonged antiseptic contact, to reduce danger of external infection by inhibiting bacterial growth, and permit clean natural healing.
UDDER MASSAGE: To promote better circulation in congested udder, apply liberally with thorough massage, removing milk at each application.
Expiration date on underside of can.
Made in U.S.A.
Spec 6016

Label
(click image for full-size original)
UDDER BALM
oxyquinoline ointment
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:15878-413
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxyquinoline (Oxyquinoline) Oxyquinoline .25 g in 1 g
Inactive Ingredients
Ingredient Name Strength
Petrolatum
Water
Lanolin
Yellow Wax
Paraffin
Clove Leaf Oil
Sodium Borate
Apocarotenal
.beta.-carotene
Isopropyl Alcohol
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:15878-413-13 255 g in 1 CAN None
2 NDC:15878-413-18 1200 g in 1 CAN None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/01/1964
Labeler — H. W. Naylor Company Inc. (002080190)
Establishment
Name Address ID/FEI Operations
H. W. Naylor Company Inc. 002080190 API MANUFACTURE, MANUFACTURE

Revised: 01/2013 H. W. Naylor Company Inc.

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