HYDROPEPTIDE SPOT CORRECTION- sulfur ointment

HydroPeptide SPOT CORRECTION by

Drug Labeling and Warnings

HydroPeptide SPOT CORRECTION by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active ingredients

Colloidal Sulfur (3%)

Purpose

Acne treatment ointment

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.

Uses

• treat acne
• helps prevent new pimples
• clears up most acne pimples
  

Warnings

For external use only

Do not use on

• broken skin
• large areas of the body
  

When applying this product

• apply only to area with acne
• rinse right away with water if it gets in eyes
• 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.
  

Stop use and ask a doctor if

skin irritation occurs or gets worse

Directions

• clean skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three times daily
• because excessive drying of the skin may occur, start with one application, then gradually increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling ocurs, reduce application to once a day or every other day
  

Other information

• store at controlled room temperature (59° - 86°F)
  

Inactive ingredients

4-t-Butylcyclohexanol, Acacia Senegal Gum, Arginine, Chondrus Crispus (Carrageenan), Citrus Grandis (Grapefruit) Peel Oil, pilobium Angustifolium Flower/Leaf/Stem Extract, Lactic Acid, Leuconostoc/radish Root Ferment Filtrate, Melaleuca Alternifolia (Tea Tree) Leak Oil, Niacinamide, Pentylene Glycol, Rice Ferment (Sake) Filtrate, Sodium Hydroxide, Water (Aqua), Xanthan Gum

Questions or comments?

Call 1-800-932-9873

HydroPeptide SPOT CORRECTION Product Label

HydroPeptide®

SPOT CORRECTION

Acne Eliminating Treatment
Anti-Wrinkle + Clarify

0.5 FL OZ / e15 mL

VRL Technology

Peptide Variety

Clinical Levels

Repetition and Layering

HydroPeptide® is the leader in anti-aging skincare with our proprietary VLR technology; using the correct variety of peptides at clinical levels with continuous repetition for superior anti-aging results

Colloidal Sulfur, Lactic Acid, Sake Peptide

This advanced formula combines acne fighting and anti-aging ingredients that clear up acne pimples and prevent new ones from forming without over-drying the affected area

GLUTEN FREE, PARABEN FREE, PHTHALATE FREE
FOR ALL SKIN TYPES, NOT TESTED ON ANIMALS

DIST. BY PREMIER HEALTHSOURCE, INC.
ISSAQUAH, WA 98027

RP. MSL, BL9 5NB, UK
MADE IN THE USA

WWW.HYDROPEPTIDE.COM

INGREDIENTS AND APPEARANCE

HYDROPEPTIDE SPOT CORRECTION 
sulfur ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-117
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	1.5 g  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)
ACACIA (UNII: 5C5403N26O)
ARGININE (UNII: 94ZLA3W45F)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
LACTIC ACID (UNII: 33X04XA5AT)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
TEA TREE OIL (UNII: VIF565UC2G)
NIACINAMIDE (UNII: 25X51I8RD4)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-117-50	15 mL in 1 TUBE; Type 0: Not a Combination Product	05/17/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	05/17/2014

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Bentley Laboratories, LLC (068351753)

Establishment
Name	Address	ID/FEI	Business Operations
Bentley Laboratories, LLC		068351753	manufacture(54111-117)