CBD BLUE LIGHT DEFENSE SPF 30- zinc oxide cream

CBD Blue Light Defense SPF 30 by

Drug Labeling and Warnings

CBD Blue Light Defense SPF 30 by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Zinc Oxide 18.90%

PURPOSE

Purpose: Sunscreen

INDICATIONS & USAGE

Uses:

• Helps prevent sunburn.
• If used as directed with other sun protection measure, this product decreases 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.

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach odf childern. If product is swallowed, get medical help or contact a posion control center right away.

DOSAGE & ADMINISTRATION

Directions:

• Apply liberally 15 minutes before sun exposure.
• Children under 6 months of age: Ask a doctor
• Reapply at least every 2 hours.

OTHER SAFETY INFORMATION

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 Specturm SPF value of 15 or higher and other sun protection measures including:

• Limit time in the sun, especially form 10 a.m. - 2:0 pm
• Wear long sleeved shirts, pants, hats and sunglasses.
• Protect the product in this container form excessive heat and direct sun.

INACTIVE INGREDIENT

Other Ingredients: Water (Aqua), Caprylic/Capric Triglyceride , Coco-Caprylate/Caprate , Cetearyl Alcohol, Glycerin , Aloe Barbadensis Leaf Juice , Coco-Glucoside, Jojoba Esters , Dipotassium Glycyrrhizate , Sodium Phytate, Alcohol, Caprylyl/Capryl Glucoside, Xanthan Gum , Sclerotium Gum, Polyhydroxystearic acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin, Cetearyl Glucoside, Butyrospermum Parkii Nut Extract , Coconut Alkanes , Tocopherol , Tetrahexyldecyl Ascorbate, Cellulose (Microsponge/Delivery System), Hydroxyapatite, Cannabidiol (From Hemp Extract) , Caesalpinia Spinosa Fruit Extract, Helianthus Annuus (Sunflower) Sprout Extract, Pyrus Malus (Apple) Fruit Extract , Sodium Benzoate, Phenoxyethanol , Ethylhexylglycerin, Propylene Glycol

PRINCIPAL DISPLAY PANEL

Msanufacture for

Dermaquest®, Inc.

Hayward, CA-94544

Made in USA

dermaquestinc.com

INGREDIENTS AND APPEARANCE

CBD BLUE LIGHT DEFENSE SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4196
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	189 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
CANNABIDIOL (UNII: 19GBJ60SN5)
CAESALPINIA SPINOSA FRUIT POD (UNII: EXY4496LWD)
APPLE (UNII: B423VGH5S9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
ISOSTEARIC ACID (UNII: X33R8U0062)
SHEANUT (UNII: 84H6HBP32L)
TOCOPHEROL (UNII: R0ZB2556P8)
HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
COCONUT ALKANES (UNII: 1E5KJY107T)
GLYCERIN (UNII: PDC6A3C0OX)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
PHYTATE SODIUM (UNII: 88496G1ERL)
ALCOHOL (UNII: 3K9958V90M)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4196-1	57 g in 1 TUBE; Type 0: Not a Combination Product	12/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	12/11/2020

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4196)