VANILLA MINT LIP BALM- lip balm stick

Vanilla Mint Lip Balm by

Drug Labeling and Warnings

Vanilla Mint Lip Balm by is a Otc medication manufactured, distributed, or labeled by Casad Company Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Active Ingredients:
Avobenzone 2.0%
Octinoxate    6.5%
Octisalate     5.0%
Octocrylene 1.5%

PURPOSE

Purpose
Avobenzone ,,,,Sunscreen
Octinoxate ,,,,,,,Sunscreen
Octisalate ,,,,,,,,Sunscreen
Octocrylene ,,,,,Sunscreen

INDICATIONS & USAGE

Uses: Helps prevent sunburn

WARNINGS

Warnings
For external use only Do not use on damaged or broken
skin Stop use and ask a doctor if rash occurs When
using this product keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:  If swallowed, get medilcal
help or contact a Poison Control center right away.

DOSAGE & ADMINISTRATION

Directions Apply liberally 15 minutes before sun exposure Use a
water resistant sunscreen if swimming or sweating Reapply at least
every 2 hours Children under 6 months of age: Ask a doctor

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 protection measures including: limit time in the sun, especially from
10a.m. - 2p.m. wear long sleeved shirts, pants, hat, and sunglasses

INACTIVE INGREDIENT

Inactive ingredients: Sunflower oil, beeswax, extra virgin olive
oil, flavor, hemp seed oil, rosemary extract, vitamin E, aloe vera.

OTHER SAFETY INFORMATION

Other Information:

Protect this product from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL

Broad Spectrum SPF 15 Sunscreen
Vanilla Mint Lip Balm

Net Wt. 0.15 oz (4.25g)

SAFETY SEAL

Dist. by:www.totallypromotional.com | CoIdwater, OH 45828

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INGREDIENTS AND APPEARANCE

VANILLA MINT LIP BALM 
lip balm stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71087-113
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.0 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6.5 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SUNFLOWER OIL (UNII: 3W1JG795YI)
YELLOW WAX (UNII: 2ZA36H0S2V)
OLIVE OIL (UNII: 6UYK2W1W1E)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
ROSEMARY OIL (UNII: 8LGU7VM393)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Product Characteristics
Color		Score
Shape		Size
Flavor	VANILLA (MINT)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71087-113-01	4.25 g in 1 TUBE; Type 0: Not a Combination Product	09/06/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	09/06/2022

Labeler - Casad Company Inc. (877343673)

Registrant - Casad Company Inc. (877343673)