Label: TETRA NOW 3%- tetracycline hcl ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 81871-101-11 - Packager: ADVANCED CLINICAL MANAGEMENT LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 2, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE(S)
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WARNINGS
FOR EXTERNAL USE ONLY.
DO NOT USE
- IF YOU HAVE AN ALLERGY TO ANY INGREDIENT
- IN THE EYES
- OVER LARGE AREAS OF THE BODY
CONSULT A DOCTOR BEFORE USE IF YOU HAVE
- DEEP OR PUNCTURE WOUNDS
- SERIOUS BURNS
- ANIMAL BITES
- DIABETES AND A WOUND ON THE FOOT
- YOU NEED TO USE LONGER THAN 1 WEEK
- CONDITIONS PERSIST OR GET WORSE
- RASH OR ALLERGIC REACTION DEVELOPS
IF PREGNANT OR BREAST-FEEDING CONSULT A DOCTOR BEFORE USE.
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- INACTIVE INGREDIENTS
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TETRA NOW 3%
tetracycline hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81871-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRACYCLINE HYDROCHLORIDE (UNII: P6R62377KV) (TETRACYCLINE - UNII:F8VB5M810T) TETRACYCLINE HYDROCHLORIDE 3 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81871-101-11 1 in 1 BOX 12/02/2021 1 7.5 g 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 part333B 12/02/2021 Labeler - ADVANCED CLINICAL MANAGEMENT LLC (118026938)