NATURAL ACNE SOLUTIONS 3 STEP REGIMEN- salicylic acid 
Burt's Bees

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredients

SALICYLIC ACID 1.0%

Purpose

Acne Treatment

PENETRATES PORES TO CONTROL ACNE.

HELPS PREVENT THE DEVELOPMENT OF NEW BLEMISHES

WARNINGS

FOR EXTERNAL USE ONLY. USING OTHER TOPICAL ACNE MEDICATION AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

Keep out of reach of children IF SWALLOWED, GET MEDICATL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

APPLY TO FACE IN THE MORNING AND EVENING AFTER CLEANSING. IF BOTHERSOME DRYNESS OCCURS, REDUCE TO ONCE A DAY OR EVERY OTHER DAY.

INACTIVE INGREDIENTS

WATER, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, GLYCERIN, STEARIC ACID, SUCROSE POLYSTEARATE, SALIX NIGRA (WILLOW) BARK EXTRACT, BEESWAX, CYMBOPOGON SCHOENANTHUS EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT, HUMULUS LUPULUS (HOPS) EXTRACT, EQUISETUM HIEMALE EXTRACT, HYDRASTIS CANADENSIS (GOLDENSEAL) EXTRACT, EPILOBIUM FLEISCHERI EXTRACT, LECITHIN, CHONDRUS CRISPUS (CARAGEENAN), FRAGRANCE, GLUCOSE, XANTHAN GUM, SUCROSE, SUCROSE STEARATE, POTASSIUM SORBATE, SODIUM CHLORIDE, GLUCOSE OXIDASE, LACTOPEROXIDASE, PHENOXYETHANOL.

QUESTIONS?

800-849-7112 OR WWW.BURTSBEES.COM

ACTIVE INGREDIENTS

SALICYLIC ACID 1.0%

PURPOSE

ACNE TREATMENT

USES

PENETRATES PORES TO CONTROL ACNE.

HELPS PREVENT THE DEVELOPMENT OF NEW BLEMISHES.

WARNINGS

FOR EXTERNAL USE ONLY. USING OTHER TOPICAL ACNE MEDICATION AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION WHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

Keep out of reach of children. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

WASH FACE IN THE MORNING AND EVENING AVOIDING THE EYE AREA. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

QUESTIONS?

800-849-7112 OR WWW.BURTSBEES.COM

INACTIVE INGREDIENTS

WATER, DECYL GLUCOSIDE, LAURYL GLUCOSIDE, SUCROSE LAURATE, SALIX NIGRA (WILLOW) BARK EXTRACT, COCO-BETAINE, BETAINE, BETA VULGARIS (BEET) ROOT EXTRACT, CENOTHERA BIENNIS (EVENING PRIMROSE) LEAF EXTRACT, SODIUM COCOYL HYDROLYZED SOY PROTEIN, HYDROXYPROPYLTRIMONIUM HONEY, GLYCERIN, GLYCERYL OLEATE, COCO GLUCOSIDE, FRAGRANCE, GLUCOSE, ALCOHOL DENAT., GLUCOSE OXIDASE, LACTOPEROXIDASE, CITRIC ACID, SODIUM CHLORIDE, PHENOXYETHANOL.

Salicylic Acid 0.75%

Acne Treatment

Uses

Warnings

For external use only. Using other topical acne medication at the same time or immediately following use of this product may increased dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

Keep out of reach of children. If swallowed, get medical help and contact a Poison Control Center right away.

Directions

Apply to face in the morning and evening after cleansing.

Inactive Ingredients

Inactive Ingredients: alcohol denat., citrus medica limonum (lemon) peel oil, water, achillea millefolium extract, borago officinalis extract, calendula officinalis flower extract, carum petroselinum (parsley) extract, foeniculum vulgare (fennel) oil, salix nigra (willow) bark extract, melaleuca alternifolia (tea tree) leaf oil, eucalyptus globulus leaf oil, juniperus communis fruit oil

Questions? 800-849-7112 or www.burtsbees.com

BURTS BEES

Natural

ACNE SOLUTIONS

1 Purifying Gel Cleanser

2 Daily Moisturizing Lotion

3 Targeted Spot Treatment

3 Step Regimen Kit Salicylic Acid Acne Treatment from Willow Bark

Acne Regimen Kit

NATURAL ACNE SOLUTIONS 3 STEP REGIMEN 
salicylic acid kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26052-035
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:26052-035-101 in 1 BOX; Type 0: Not a Combination Product01/02/2014
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 10 BOTTLE, PLASTIC 1 mL  in 100 
Part 20 BOTTLE, WITH APPLICATOR 1 g  in 100 
Part 30 BOTTLE, PUMP 1 g  in 100 
Part 1 of 3
NAS PURIFYING CLEANSER 
salicylic acid gel
Product Information
Item Code (Source)NDC:26052-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERYL OLEATE (UNII: 4PC054V79P)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
SUCROSE LAURATE (UNII: 05Q7CD0E49)  
COCO GLUCOSIDE (UNII: ICS790225B)  
GLUCOSE OXIDASE (UNII: 0T8392U5N1)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYPROPYLTRIMONIUM CHLORIDE FRAGMENT (UNII: N30M4819DB)  
BETA VULGARIS (UNII: 4G174V5051)  
HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)  
ALCOHOL (UNII: 3K9958V90M)  
LACTOPEROXIDASE BOVINE (UNII: 01UIN5OC49)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
SALIX NIGRA BARK (UNII: QU52J3A5B3)  
COCO-BETAINE (UNII: 03DH2IZ3FY)  
BETAINE (UNII: 3SCV180C9W)  
OENOTHERA BIENNIS LEAF (UNII: 153YBS895W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:26052-010-02145 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D02/01/2010
Part 2 of 3
NAS TARGETED SPOT TREATMENT 
salicylic acid liquid
Product Information
Item Code (Source)NDC:26052-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.75 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
LEMON OIL (UNII: I9GRO824LL)  
BORAGO OFFICINALIS SEED (UNII: 2GXJ790US0)  
PARSLEY OIL (UNII: IXK9N7RJ7J)  
SALIX NIGRA BARK (UNII: QU52J3A5B3)  
TEA TREE OIL (UNII: VIF565UC2G)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
FENNEL OIL (UNII: 59AAO5F6HT)  
JUNIPER BERRY OIL (UNII: SZH16H44UY)  
ALCOHOL (UNII: 3K9958V90M)  
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:26052-011-037.5 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D02/01/2010
Part 3 of 3
NAS DAILY MOISTURIZING 
salicylic acid lotion
Product Information
Item Code (Source)NDC:26052-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
LEVOGLUCOSE (UNII: 02833ISA66)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
EPILOBIUM FLEISCHERI WHOLE (UNII: 8E2KLS8J8K)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
GLYCERIN (UNII: PDC6A3C0OX)  
SALIX NIGRA BARK (UNII: QU52J3A5B3)  
WHITE WAX (UNII: 7G1J5DA97F)  
CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W)  
HUMULUS LUPULUS WHOLE (UNII: 912A6Q1N4A)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SUCROSE STEARATE (UNII: 274KW0O50M)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLUCOSE OXIDASE (UNII: 0T8392U5N1)  
EQUISETUM HYEMALE (UNII: 59677RXH25)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)  
SUCROSE (UNII: C151H8M554)  
LACTOPEROXIDASE BOVINE (UNII: 01UIN5OC49)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:26052-012-0155 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/02/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/02/2014
Labeler - Burt's Bees (613480946)

Revised: 4/2016
Document Id: 3165a1c3-b39e-0faa-e054-00144ff8d46c
Set id: 310198a7-eb46-57e6-e054-00144ff88e88
Version: 2
Effective Time: 20160426
 
Burt's Bees