OH MY BOD LIGHT SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion

Oh My Bod Light Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Oh My Bod Light Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by Baxter Laboratories Pty. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Avobenzone 3% Sunscreen

Homosalate 10% Sunscreen

Octisalate 5% Sunscreen

Octocrylene 8% Sunscreen

PURPOSE

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

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.

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

Warnings

• For external use only
• Do not use on damaged or broken skin
• When using this product keep out of eyes, rinse with water to remove

DOSAGE & ADMINISTRATION

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

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

• Limit time in the sun, especially from 10 a.m.- 2 p.m.
• Wear long-sleeved shirts, pants, hats, and sunglasses.
• Children under 6 months: Ask a doctor.

INACTIVE INGREDIENT

Inactive ingredients

Water, Cera Alba, C12-15 Alkyl Benzoate,PEG-15 Cocamine, Silica, Sodium Hyaluronate, Alteromonas Ferment Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Carthamus Tinctorius (Safflower) Seed Oil, Cucumis Sativus (cucumber) Fruit Extract, Camellia Sinensis (Green Tea) Leaf Extract, Aloe Barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate, Caprylyl Glycol, PEG-40 Stearate, Butylene Glycol, Hydroxyethylcellulose, Carbomer, Caprylhydroxamic Acid, Glycerin, Triethanolamine, Potassium Sorbate, Citric acid, Fragrance.

OTHER SAFETY INFORMATION

Other information

• Protect the product in this conainer from excessive heat and direct sun
• Store below 86ºF/30ºC

PRINCIPAL DISPLAY PANEL

Everyday Humans

SPF 50

Oh my Bod

Light Sunscreen Lotion

Broad Spectrum UVA/UVB

Water Resistant (80 Minutes)

3.4 FL. OZ - 100 ML

INGREDIENTS AND APPEARANCE

OH MY BOD LIGHT SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70157-033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	8 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SILICA (UNII: ETJ7Z6XBU4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
WHITE WAX (UNII: 7G1J5DA97F)
PEG-15 COCAMINE (UNII: 8L6LB12TSJ)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
PEG-40 STEARATE (UNII: ECU18C66Q7)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CARBOMER (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID (UNII: 2968PHW8QP)
ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z)
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL (UNII: 65UEH262IS)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
JOJOBA OIL (UNII: 724GKU717M)
CUCUMIS SATIVUS (CUCUMBER) FRUIT (UNII: YY7C30VXJT)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70157-033-01	100 mL in 1 TUBE; Type 0: Not a Combination Product	09/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/30/2024

Labeler - Baxter Laboratories Pty. Ltd. (740537709)