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

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Babyganics

Autumn Harp, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Active Ingredients                                                      Purpose

Octinoxate 7.5%, Octisalate 5.0%, Zinc Oxide 11.2%     Sunscreen

Babyganics Uses

Uses

helps prevent sunburn

if used as directed with other sun protection measures (see Directions), decrease the risk of skin cancer and early skin aging caused by the sun

Warnings

Warnings

For external use only

Do not use

Do not use on damaged or broken skin

When using this product

When using this product keep out of eyes, Rinse with water to remove.

Stop use and ask a doctor

Stop use and ask a doctor if rash occurs

Keep out of reach of children

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

apply liberally 15 minutes before sun exposure

reapply

after 80 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

children under 6 months of age: ask a doctor

Sun Protection Measures

Sun Protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk of skin cancer and early skin aging. To decrease this risk sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

limit time in the sun, especially from 10 am - 2 pm.

wear long-sleeved shirts, pants, hats, andsunglasses

Other Information

Other information

protect from excessive heat and direct sun

Inactive ingredients

Inactive Ingredients:  Water, Glycerin, Caprylic/Capric Triglyceride, Aloe Barbadensis Leaf Juice, VP/hexadecene copolymer, Cetearyl Glucoside, Phenethyl Alcohol, Glyceryl Caprylate, Polyacrylate Crosspolymer-6, Cetearyl Alcohol, Citric Acid.

Label

Babyganics

Babyganics

Octinoxate, Octisalate, and Zinc SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51514-0235
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 11.2 mL
OCTINOXATE OCTINOXATE 7.5 mL
OCTISALATE OCTISALATE 5.0 mL

Inactive Ingredients

Ingredient Name Strength
water
Aloe Vera Leaf
CITRIC ACID MONOHYDRATE
GLYCERIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51514-0235-1 177 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-02-23


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