INDICATIONS     CONTRA-INDICATIONS     DOSAGE     SIDE-EFFECTS     PREGNANCY     OVERDOSE     IDENTIFICATION     PATIENT INFORMATION
SB UNIVERSAL OINTMENT

SCHEDULING STATUS:
Non-scheduled

PROPRIETARY NAME
(and dosage form):

SB UNIVERSAL OINTMENT

COMPOSITION
Each 25 g contains:

Starch		2,498 g
Zinc Oxide		3,749 g
Coal Tar Solution		1,878 mL
Phenol		0,47 g
Cod Liver Oil		1,879 mL

PHARMACOLOGICAL CLASSIFICATION
A 13 4 Dermatological Preparations - Antipruritics

PHARMACOLOGICAL ACTION:
Antipruritis and Antieczematous.

INDICATIONS:
For the relief of minor eczematous conditions, associated with itching, and minor dermatitis.

CONTRA-INDICATIONS:
Hypersensitivity to any of the ingredients.
In any severe skin condition it is recommended that a dermatologist be consulted.

DOSAGE AND DIRECTIONS FOR USE:
Wash and dry the affected area, and apply Universal Ointment three times daily.

SIDE-EFFECTS AND SPECIAL PRECAUTIONS:
For external use only.
If the condition persists, discontinue use and consult your doctor.

IDENTIFICATION:
Beige Ointment

PRESENTATION:
25 g jar

STORAGE INSTRUCTIONS:
Store in a cool, dry place below 25°C and away from light. Keep out of reach of children.

REFERENCE NO:
G1935 (Wet/Act 101/1965)

NAME AND BUSINESS ADDRESS OF THE APPLICANT:
Universal Pharmaceuticals (Pty) Ltd.
7 Browning Street, Jeppe, Johannesburg.

DATE OF PUBLICATION OF THIS PACKAGE INSERT:
2 November 1974

                Code SB15I
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