LIP BALM description, usages, side effects, indications, overdosage, supplying and lots more!

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LIP BALM

Kamins Dermatologics Inc.
Kamins Dermatologics Inc.

CONSUMER LABELING




FULL PRESCRIBING INFORMATION

Active ingredient



OCTINOXATE 7.5 %

OXYBENZONE 5 %

ZINC OXIDE 4 %

Purpose



Uses


A soothing treatment balm that helps heal and protect lips from sun, wind and extreme tempera- tures. Repairs happed, sore lips with Bio-MapleTM compound and skin softening oils. Also helps prevent the breakout of lip sores with broad spectrum UVA/UVB sun screening agents. Creates a smoother palette for lipstick application by diminishing the appearance of lip lines and reducing the feathering of lip color. Use anytime for fuller, more luscious lips

Uses

helps prevent sunburn

higher SPF gives more sunburn protection

provides moderate protection against sunburn

Warnings

For external use only.

When using this product, keep out of eyes. If contact occurs, rinse abundantly with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

If swallowed, seek medical assistance or contact a Poison Control Center immediately.



Sun alert: limiting sun exposure, earing protective clothing and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.





Directions

Using the angled tube applicator, squeeze tube and apply directly to lips 15-30 minutes before sun exposure. Reapply as needed, especially after prolonged sun exposure, drinking or eating.

Children under 6 months of age: ask a doctor.




Polybutene, ricinus communis (castor) seed oil, petrolatum, VP/hexadecene copolymer, cera alba (beeswax), cyclopentasiloxane/dimethicone crosspolymer, caprylic/capric triglyceride, squalane, copernicia cerifera (carnauba wax), paraffin, tocopheryl acetate, acer saccharum (maple isolate), flavour/aroma, benzyl benzoate

B. KAMINS

LIP BALM SPF 20

15 G / 0.5 fl.oz

DIN 02248084

LIP BALM

LIP BALM

OCTINOXATE OXYBENZONE ZINC OXIDE OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63550-114
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
OXYBENZONE OXYBENZONE 50 mg
Zinc Oxide Zinc oxide 40 mg

Inactive Ingredients

Ingredient Name Strength
POLYBUTENE (1400 MW)
castor oil
petrolatum
1-HEXADECENE
white wax
CYCLOMETHICONE 5
DIMETHICONE
TRICAPRIN
TRICAPRYLIN
SQUALANE
carnauba wax
PARAFFIN
ALPHA-TOCOPHEROL ACETATE
ACER SACCHARUM SAP
Benzyl Benzoate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63550-114-01 15 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-03-07


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