BUTT AND THIGHS

Manufacturer
Teamtrade Inc.
Effective date
2023-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:58:44

Label at a glance#

ProductBUTT AND THIGHS ACNE TREATMENT
Active ingredientSALICYLIC ACID
Label structure13 sections

Dosage and administration

Clean the skin thoroughly before applying product. Cover the entire affected area with a thin layer one to three times daily. Because excess drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

OTC - PURPOSE SECTION

Purpose: Acne treatment

USE:

INDICATIONS & USAGE SECTION

For the treatment of acne.

WARNINGS SECTION

For external use only.

Do not use on children under 12 years of age unless directed by a doctor.

OTC - STOP USE SECTION

Stop use and consult a doctor if

Condition worsens or does not improve with regular use of this product as directed.

OTC - WHEN USING SECTION

Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding Consult a health care professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Clean the skin thoroughly before applying product.
Cover the entire affected area with a thin layer one to three times daily.
Because excess drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.

If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

OTHER SAFETY INFORMATION

See on the top of the tube for lot number and expiration date.

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

INACTIVE INGREDIENT SECTION

Aqua, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Caprylic/Capric Triglyceride, Beeswax, Glycerin, Polyglyceryl-6 Palmitate/Succinate, Cetearyl Alcohol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Cetyl Alcohol, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol, Organic Butyrospermum Parkii (Shea) Butter, Dimethicone, Dimethicone Crosspolymer, Aloe Barbadensis (Aloe Vera) Leaf Juice, Parfum, Sodium Hydroxide, Xanthan Gum, Disodium EDTA, Rosmarinus Officinalis (Rosemary) Extract, Tocopheryl Acetate, Mentha Piperita (Peppermint) Oil, Salix Alba Bark Extract, Camellia Sinensis Leaf Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Hexyl Cinnamal, D-Limonene, Linalool, Benzyl Salicylate, Benzyl Alcohol, Citral.

OTC - QUESTIONS SECTION

Call (1-877-737-6267)

BUTT & THIGHS ACNE TREATMENT CREAM 4oz (Label - Box)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SEROFLORA BUTT AND THIGHSSEROFLORA BUTT AND THIGHS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
317152salicylic acid 2 % Topical CreamPSN3
317152salicylic acid 20 MG/ML Topical CreamSCD3
317152salicylic acid 2 % Topical CreamSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82767-002-04BUTT AND THIGHSACNE TREATMENT118.3 mL in 1 TUBECREAM118.33

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82767-002BUTT AND THIGHS ACNE TREATMENT (SALICYLIC ACID) CREAM [TEAMTRADE INC.]3Legacy NDC, 1 package rows20231103_e94a3d17-564f-3e64-e053-2995a90aa402.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82767-00282767-002-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
08025e53-5dc0-37f7-e063-6394a90a50c9e94a3d17-564f-3e64-e053-2995a90aa4022023-10-18WarningsExact identifier
spl id: 08025e53-5dc0-37f7-e063-6394a90a50c9
spl set id: e94a3d17-564f-3e64-e053-2995a90aa402

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.