HABIT SPF 41- facial spray

Habit by

Drug Labeling and Warnings

Habit by is a Otc medication manufactured, distributed, or labeled by Bell International Laboratories, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Avobenzone 2.8%

Homosalate 9.8%

Octisalate 4.9%

Octocrylene 9.5%

Purpose

Sunscreen

Uses

Helps prevent sunurn

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.

Warnings

For external use only

Do not use on damaged or broken skin

When using this producty keep out of eyes. Rinse wtih water to remove.

Stop use and ask a doctor if rash occurs

Flammable. Keep away from fire or spark.

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

Apply generously 15 minutes before sun exposure

Reapply at least every 2 hours

Use a warer-resistant sunscreen if swimming or sweating

Reapply after swimming or sweating

Children under 6 monts-age: Ask a doctor

Sun Protection Meaures. 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 10a.m. - 2 p.m.

-wear long-sleeved shirts, pants, hats, and sunglasses.

Other Information

Protect the product in this container from excessive heat and direct sun

Inactive Ingredients

Alcohol Denat., Bisabolol, Butyloctyl Salicylate, Capryloyl Glycerin/Sebacic Acid Copolymer, Dicaprylyl Ether, Diheptyl Succinate, Diisooctyl Succinate, Ethyl Ferulate, Isononyl Isononanoate, Lavendula Augustifolia (Lavender) Oil, Pelargonium Graveolens Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil

package label

INGREDIENTS AND APPEARANCE

HABIT  SPF 41
facial spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-261
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.9 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.8 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9.8 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
DICAPRYLYL ETHER (UNII: 77JZM5516Z)
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
LEVOMENOL (UNII: 24WE03BX2T)
ROSEMARY (UNII: IJ67X351P9)
ETHYL FERULATE (UNII: 5B8915UELW)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALCOHOL (UNII: 3K9958V90M)
DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-261-51	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/01/2020

Labeler - Bell International Laboratories, Inc (967781555)