SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER- sulfur ointment

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)

Available from:

J. Strickland & Co.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Controls scalp itching and flaking due to dandruff

Authorization status:

OTC monograph final

Summary of Product characteristics

SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER-
SULFUR OINTMENT
J. STRICKLAND & CO.
----------
SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER
_ACTIVE INGREDIENTS_
Sulfur, 2%
_PURPOSE_
Antidandruff
_USE:_
Controls scalp itching and flaking due to dandruff
_WARNINGS:_
For external use only
WHEN USING THIS PRODUCT
do not get into eyes. If contact occurs, rinse eyes thoroughly with
water.
STOP USE AND ASK A DOCTOR IF
condition worsens or does not improve after regular use.
IF SWALLOWED, GET MEDICAL HELP OR CALL A POISON CONTROL CENTER AT
ONCE.
a gradual blue-black darking of the skin occurs
irritation becomes severe
no improvement is seen after 3 months
_DIRECTIONS_
Apply to the affected area 1 - 4 times daily, or as directed by a
doctor
_INACTIVE INGREDIENTS_
Petrolatum, Lanolin, Mineral Oil, Menthol, Fragrance, Yellow 11.
12022-018-00
12022-018-01
12022-018-02
SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER
sulfur ointment
J. Strickland & Co.
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:12022-018
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)
SULFUR
20 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
MENTHOL (UNII: L7T10EIP3A)
D&C YELLOW NO. 11 (UNII: 44F3HYL954)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:12022-018-
00
57 g in 1 JAR; Type 0: Not a Combination
Product
12/01/1990
2
NDC:12022-018-
01
113 g in 1 JAR; Type 0: Not a Combination
Product
12/01/1990
3
NDC:12022-018-
02
205 g in 1 JAR; Type 0: Not a Combination
Product
12/01/1990
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M032
12/01/1990
LABELER -
J. Strickland & Co. (007023112)
REGISTRANT -
J. Strickland & Co. (007023112)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUS