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NDC 49035-0934-83 Quick Action 2 g/100mL Details

Quick Action 2 g/100mL

Quick Action is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Equate. The primary component is SALICYLIC ACID.

MedlinePlus Drug Summary

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.

Related Packages: 49035-0934-83
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Salicylic Acid Topical

Product Information

NDC	49035-0934
Product ID	49035-934_eb8925fd-dceb-46e3-8518-e66530076c96
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Quick Action
Proprietary Name Suffix	n/a
Non-Proprietary Name	Salicylic acid
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	TOPICAL
Active Ingredient Strength	2
Active Ingredient Units	g/100mL
Substance Name	SALICYLIC ACID
Labeler Name	Equate
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333D
Listing Certified Through	2024-12-31

Package

Package Images

NDC 49035-0934-83 (49035093483)

Pricing Information	N/A
NDC Package Code	49035-934-83
Billing NDC	49035093483
Package	200 mL in 1 TUBE (49035-934-83)
Marketing Start Date	2017-06-21
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 00025ea5-d15f-49d2-a52a-6c1bd8c6a033 Details

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Uses

for the treatment of acne

Warnings

For external use only

When using this product

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.

Keep out of reach of children

If swallowed get medical help or contract a Poison Control Center right away

Directions

wet face, apply to hand, massage face gently. Rinse well. Use up to twice daily
avoid contact with eyes. If contact occurs, flush thoroughly with water.

Inactive ingredients

water, sodium cocoyl isethionate, cetearyl alcohol, laureth-3, glycerin, coconut acid, sodium isethionate, sodium hydroxide, fragrance, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract, disodium EDTA

questions?

1-888-287-1915

disclaimer

Satisfaction guaranteed-Or we'll replace it or give you your money back. For Questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915

This product is not manufactured or distributed by Reckitt Benckser, distributor of Clearasil ULTRA Rapid Action Daily Face Wash.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY:

Wal-Mart Stores, Inc.,

Bentonville, AR 72716

580.000/580AA

principal display panel

equate beauty

COMPARE TO CLEARASIL ULTRA RAPID ACTION DAILY FACE WASH*

QUICK ACTION DAILY FACE WASH

Salicylic acid 2% acne treatment

Noticeably clearer skin

Dermatologist tested

PARABEN FREE

6.78 FL OZ (200 mL)

INGREDIENTS AND APPEARANCE

QUICK ACTION

salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-934
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
LAURETH-3 (UNII: F32E4CB0UJ)
GLYCERIN (UNII: PDC6A3C0OX)
COCONUT ACID (UNII: 40U37V505D)
SODIUM ISETHIONATE (UNII: 3R36J71C17)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
CISTUS MONSPELIENSIS WHOLE (UNII: T2OG06826L)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-934-83	200 mL in 1 TUBE; Type 0: Not a Combination Product	06/21/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	06/21/2017

Labeler - Equate (051957769)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(49035-934)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(49035-934)

Revised: 9/2022

Document Id: eb8925fd-dceb-46e3-8518-e66530076c96

Set id: 00025ea5-d15f-49d2-a52a-6c1bd8c6a033

Version: 12

Effective Time: 20220902