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Viquin
is used to temporarily fade dark skin spots such as freckles and
Side Effects:
This medication may cause dry skin, burning or redness.
Notify your doctor if you develop any of these symptoms.
In the unlikely event you have an allergic reaction to this drug,
seek medical attention immediately.
Symptoms of an allergic reaction include rash, itching, swelling,
dizziness or trouble breathing.
Precautions:
:Tell your doctor if you have any pre-existing illness, infections
or allergies, especially to sulfites or sunscreens.
This medication should be used only if clearly needed during pregnancy.
Discuss the risks and benefits with your doctor.
It is not known if this medication is excreted into breast milk.
Consult your doctor before breast-feeding.

Generic Name: Sunscreen/Hydroquinone
Related:
Eldopaque Forte 4% Cream - Prescription
Viquin Forte 4% Cream - Prescription
Alphaquin HP 4% Cream - Prescription
Eldopaque 2% Cream - Over the counter
mdhs98
Employers are required to make an assessment of the health
risk created by such work, and to prevent or control exposure to
the substances involved.
3 Exposure to hydroquinone can cause skin irritation and sensitisation,
and irritation to the eyes, nose and throat.2 Hydroquinone has also
been shown to be mutagenic in animals and a no-adverse-effect-level
cannot be identified in humans.
100 Asbestos-containing materials © Crown copyright 2003 Applications
for reproduction should be made in writing to: Copyright Unit, Her
Majesty's Stationery Office, St Clements House, 2-16 Colegate, Norwich
NR3 1BQ All rights reserved.
No part of this publication may be reproduced, stored in a retrieval
system, or transmitted in any form or by any means (electronic,
mechanical, photocopying, recording or otherwise) without the prior
written permission of the copyright owner. measurements, water.
reg2083
2. (1) Subject to the provisions of subregulation (2), no person,
shall sell (a) a cosmetic which contains lead or its salts, hydroquinone
monobenzyl ether (p-hydroxyphenyl benzyl ether or monobenzone),
or mercury or its salts; or (b) a cosmetic as a skin lightening
agent or skin whitener, or a cosmetic purporting to be a skin lightening
agent or skin whitener, which (i) contains any active or petentially
depigmenting ingredient other than hydroquinone; (ii) contains more
than 2 per cent hydroquinone by volume or mass, whichever is the
greater in a specific preparation; (iii) contains catechols, salicylic
acid, methyl salicylate, trimethyl cyclohexanol, resorcinol, oxyquinoline,
sulphate, odochlorohydroxyquin, thymol, hexachlorophene and other
phenolic compounds; (iv) does not contain a sun screen with a protection
factor (SPF) of 5 or an equivalent sun blocking agent in the finished
product; or (c) any cosmetic which contains hydroquinone other than
a cosmetic referred to in paragraph (b); or (d) any cosmetic designated
as "Blue Butter", "Blue Ointment" or "Blou
Botter". cosmetics, salicylate.
5004
OTHER METHODS: This is Method S57 [2] in a revised format.
The equilibrium vapor pressure is equivalent to 0.11 mg/m 3 at 25
°C and may be a significant factor at elevated temperatures.
Immediately after sampling, transfer the filter (do not include
backup pad) with tweezers to a 60-mL ointment jar.
Check recovery with at least three spiked media blanks per sample
set.
The atmospheres were generated by atomization of an aqueous solution
of hydroquinone into dry air; aerosol concentrations were independently
verified by direct UV spectrophotometry on filter samples.
Average collection efficiency was 100% at 4 mg/m loss of hydroquinone
was seen from filters spiked with 720 µg hydroquinone, and
then used to sample 180 L clean air, indicating the hydroquinone
vapor pressure is not significant at these conditions. hydroquinone,
recovery.
03p-0365-pdn00002-vol1.pdf
Your petition was filed on August 13,2003 and requested
permission to file an Abbreviated New Drug Application (ANDA) for
the following drug product: Hydroquinone and Tretinoin Topical Solution,
4%/0.01%.
Your request involves a change from one active ingredient to another
active ingredient in the same pharmacologic or therapeutic class
from that of the listed combination drug product (i.e., to Hydroquinone
4%).
The Agency has determined that your proposed change in active ingredient
raises questions of safety and effectiveness, and has concluded
that clinical trials are required for these specific drug products.
If there is additional information, not included as part of your
original submission that you would like the Agency to consider,
you should submit a new petition including all the necessary information
to the Dockets Management Branch. drug product, proposed drug products.
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