Life Extension Sun Protection SPF 30 description, usages, side effects, indications, overdosage, supplying and lots more!

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Life Extension Sun Protection SPF 30

LifeExtension Foundation

Life Extension Sun Protection Spray With Beta Glucan SPF 30




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Active Ingredients

Octinoxate 7.5%, Benzophenone-3 5.0%, Octisalate 3.0%, Avobenzone 0.65%

Purpose

Purposes: Sunscreen

Uses

Uses

  • Helps prevent sunburn
  • Higher SPF gives more sunburn protection
  • Provides high protection against sunburn and tanning

Warnings

  • When using this product, keep out of eyes.
  • Rise with water to remove
  • Stop use and consult a physician if rash or irritation develops
  • Keep out or reach of children

Directions

  • Apply evenly over the body before sun exposure and as needed
  • Children under 6 months of age; consult a physician
  • Reapply as needed or after towel drying, swimming, or perspiring

Inactive Ingredients

SD-Alcohol 40B, Ethyl Ester of PVM/MA Copolymer, Aloe Extract, Oat Beta Glucans, Tocopherol Acetate (Vitamin E), Polysorbate-20, Cucumber Extract, Chamomile, Sodium PCA (NaPCA), Retinyl Palmitate (Vitamin A), Ascorbyl Palmitate (Vitamin C), Fragrance, DMDM Hydantoin.

Other Information: High sun protection product. Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful  effects of the sun.

Questions or comments?

1-800-544-4440

Manufactured for:

Quality Supplements and Vitamins, Inc.

Ft. Lauderdale, Fl 33309

email: info@lifeextension.com

website: http: // wwww.lef.org

To report a serious adverse event or obtain product information, contact 1-866-280-2852


Life Extension

Sun

Protection

Spray

WITH BETA GLUCAN

Protects against

UV-A and UV-B

SPF 30

NET WT 6 OZ (178 ml)


Life Extension Sun Protection SPF 30

Life Extension Sun Protection SPF 30

OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76021-100
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7.5 mL
OXYBENZONE OXYBENZONE 5 mL
OCTISALATE OCTISALATE 3 mL
AVOBENZONE AVOBENZONE 0.65 mL

Inactive Ingredients

Ingredient Name Strength
ETHYL NITRATE
ALOE
OAT
ALPHA-TOCOPHEROL
POLYSORBATE 20
CUCUMBER
CHAMOMILE
SODIUM PYRROLIDONE CARBOXYLATE
ASCORBYL PALMITATE
DMDM HYDANTOIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76021-100-06 178 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-02-10


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