NO7 FUTURE RENEW DAMAGE REVERSAL DAY CREAM SUNSCREEN BROAD SPECTRUM SPF 25- avobenzone, octinoxate, octisalate, octocrylene cream

No7 Future Renew Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 by

Drug Labeling and Warnings

No7 Future Renew Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 by is a Otc medication manufactured, distributed, or labeled by BCM Ltd, The Boots Company PLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Carton Active Ingredients Section

Active ingredients

Avobenzone 3%

Octinoxate 0.5%

Octisalate 5%

Octocrylene 7.5%

Uses

Uses - helps prevent sunburn

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.

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.

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 at least every 2 hours.

use a water resistant sunscreen if swimming or sweating.

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 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

Directions

Directions

apply liberally 15 minutes before sun exposure.

reapply at least every 2 hours.

use a water resistant sunscreen if swimming or sweating.

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 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

Storage

Other information

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

avoid contact with fabrics

Inactive ingredients

Aqua (Water), Dibutyl adipate, Glycerin, Polyglyceryl-3 methylglucose distearate, VP/eicosene copolymer, Capryloyl glycerin/sebacic acid copolymer, Tribehenin, Niacinamide, Dimethicone, Ammonium acryloyldimethyltaurate/VP copolymer, Butyrospermum parkii (Shea) butter, Tocopheryl acetate, Phenoxyethanol, Panthenol, Potassium cetyl phosphate, Caprylyl glycol, Parfum (fragrance), Dimethiconol, Sodium Benzoate, Sodium Hyaluronate, Ethylhexylglycerin, Hydrolyzed rice protein, Propylene glycol, Dipropylene glycol, Ascorbyl glucoside, Citric acid, Tetrasodium EDTA, T-butyl alcohol, Propanediol, Pentylene Glycol, Decyl glucoside, Morus alba leaf extract, BHT, Palmitoyl tetrapeptide-94, Palmitoyl tetrapeptide-95

INFORMATION FOR PATIENTS

USA: Questions? 1-866-75-BOOTS

The Boots Company PLC Nottingham England NG2 3AA

Boots Retail Ireland Dublin 12 Ireland

Dist. in the USA by Boots Retail USA Inc. New York NY 10007

Made in the UK

www.no7beauty.com

Description

No7 Future RenewTM Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25

Targets and helps prevent visible signs of skin damage

50 ml e 1.69 US Fl. Oz.

Powered by PEPTICOLOYTM, No7's exclusive Peptide innovation, developed by world-leading scientists. This cutting-edge, patent-pending technology supports skin's natural self-repair.

Dermatologist approved

For best results: Use every morning, massage in small upward circles over your face & neck.

Proven to protect against UV and reverse visible signs of skin damage

Suitable for Sensitive Skin

Carton

INGREDIENTS AND APPEARANCE

NO7 FUTURE RENEW DAMAGE REVERSAL DAY CREAM SUNSCREEN BROAD SPECTRUM SPF 25 
avobenzone, octinoxate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11489-196
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.5 g  in 50 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.25 g  in 50 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3.75 g  in 50 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.5 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE (UNII: W19EIO0DBE)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
DIMETHICONE (UNII: 92RU3N3Y1O)
NIACINAMIDE (UNII: 25X51I8RD4)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SHEA BUTTER (UNII: K49155WL9Y)
PANTHENOL (UNII: WV9CM0O67Z)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
EDETATE SODIUM (UNII: MP1J8420LU)
PROPANEDIOL (UNII: 5965N8W85T)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
MORUS ALBA LEAF (UNII: M8YIA49Q2P)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PALMITOYL TETRAPEPTIDE-94 (UNII: Z6T2ETB7SH)
PALMITOYL TETRAPEPTIDE-95 (UNII: MJN3TLA2BW)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11489-196-02	1 in 1 CARTON	08/31/2023
1		50 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/31/2023

Labeler - BCM Ltd (230780322)

Registrant - The Boots Company PLC (218622660)

Establishment
Name	Address	ID/FEI	Business Operations
BCM Ltd		230780322	manufacture(11489-196) , analysis(11489-196)