Superdrug Ultra Thin Condoms 30's

Important information for natural rubber
latex condoms, please read carefully.
Always handle the condom carefully including
removal from the package so as to avoid
damage to the condom by finger nails,
jewellery, etc. If condom foil is damaged
discard that condom and use a new
undamaged one. Condoms made from natural
rubber latex may cause allergic reactions
including anaphylactic shock. A condom should
never be used for a second time, condoms are
for single use and if reused there might be an
increased risk of failure or infection, the risk of
breakage is also higher. The use of a condom
cannot guarantee 100% protection against
pregnancy, HIV, or Sexually Transmitted
Infections (STIs). If in doubt always consult a
doctor. If additional lubricant is desired, use the
type of lubricant recommended for use with
condoms e.g. for Natural Rubber Latex
Condoms a water-based lubricant such as
Pasante Light Lube. Avoid the use of oil based
lubricants, such as petroleum jelly, baby oil,
body lotions, massage oils, butter, margarine,
etc., as these are deleterious to the integrity of
the latex condom. Use of condom during anal
sex increases the risk of breakage. It is
recommended to use additional lubrication if
vaginal lubrication is insufficient or for anal sex
to minimize the risk of condom breaking or
coming off. Consult a doctor or pharmacist
about the compatibility of topical medicines that
might come in contact with the condom.
Carrying condoms in your wallet, back pocket,
handbag, or similar is not advisable. If you
have unprotected sex or your method of
contraception has failed, contact your Sexual
Health Clinic or GP for emergency
contraception advice preferably no later than
72 hours. Keep away from children, children
can choke or suffocate on uninflated or broken
condom fragments. Use of condom during oral
sex increases the risk of asphyxiation, choking
or condom breaking. A latex condom is a
medical device. The device is intended to be
used by adult lay persons. Any serious incident
that has occurred in relation to the device
should be reported to the manufacturer and the
competent authority of the Member State in
which the user and/or patient is established.