GOLD MOUNTAIN BEAUTY DRYING- salicylic acid suspension

Gold Mountain Beauty Drying by

Drug Labeling and Warnings

Gold Mountain Beauty Drying by is a Otc medication manufactured, distributed, or labeled by RENU LABORATORIES, INC., Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2 percent

PURPOSE

Topical Acne Treatment

Uses

• for the treatment of acne
• healing and drying acne breakouts
• helps clear acne pimples, blackheads or whiteheads and allows skin to heal
• penetrates pores to control acne blemishes
• helps keep skin clear of new acne pimples

WARNINGS

Warnings

For external use only

• 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.

DO NOT USE

Do Not Use

• on broken skin
• on large areas of the skin
• if pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION

Directions

• do not shake
• clean skin thoroughly before applying this product
• carefully place wand or cotton swab into sediment at bottom and apply directly to blemish
• because excessive 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

INACTIVE INGREDIENT

Camphor, Deionized Water, Hippophae Rhamnoides (Sea Berry) Fruit and Seed Oil, Iron Oxide, Isopropyl Alcohol, Magnesium Aluminum Silicate, Sulfur, Zinc Oxide

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

PRINCIPAL DISPLAY PANEL

LABEL AND BOX ART FOR DRYING LOTION

INGREDIENTS AND APPEARANCE

GOLD MOUNTAIN BEAUTY DRYING 
salicylic acid suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-461
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.56 g  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
ZINC OXIDE (UNII: SOI2LOH54Z)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SULFUR (UNII: 70FD1KFU70)
CAMPHOR, (-)- (UNII: 213N3S8275)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-461-02	1 in 1 BOX	01/04/2021
1	NDC: 76348-461-01	28 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	01/04/2021

Labeler - RENU LABORATORIES, INC. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories, Inc.		945739449	manufacture(76348-461)