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NDC 69968-0013-05 Clean and Clear acne triple clear exfoliating scrub 20 mg/g Details

Clean and Clear acne triple clear exfoliating scrub 20 mg/g

Clean and Clear acne triple clear exfoliating scrub is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. 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: 69968-0013-05
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Salicylic Acid Topical

Product Information

NDC	69968-0013
Product ID	69968-0013_edf589c4-e913-5cfa-e053-2995a90ae311
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	Clean and Clear acne triple clear exfoliating scrub
Proprietary Name Suffix	n/a
Non-Proprietary Name	Salicylic Acid
Product Type	HUMAN OTC DRUG
Dosage Form	GEL
Route	TOPICAL
Active Ingredient Strength	20
Active Ingredient Units	mg/g
Substance Name	SALICYLIC ACID
Labeler Name	Johnson & Johnson Consumer Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333D
Listing Certified Through	2024-12-31

Package

NDC 69968-0013-05 (69968001305)

Pricing Information	N/A
NDC Package Code	69968-0013-5
Billing NDC	69968001305
Package	141 g in 1 TUBE (69968-0013-5)
Marketing Start Date	2016-11-01
NDC Exclude Flag	N