ACNE CLEANSING SALICYLIC ACID 20 mg/mL Gel — NDC 49527-045-01 (Billing 49527-0045-01)
This is a package of ACNE CLEANSING SALICYLIC ACID 20 mg/mL Gel from CLINIQUE LABORATORIES LLC, marketed since Oct 2014 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 49527-045-01 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 49527 labeler · 045 product · 01 package
- Package marketed since
- Oct 1, 2014
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 4952704501 0
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
This is a topical gel containing salicylic acid, an over-the-counter monograph product sold without individual FDA approval but under established category rules. Salicylic acid is commonly used in acne cleansing products to help dissolve excess skin oil and dead skin cells on the skin surface. The gel formulation allows the active ingredient to be applied directly to affected areas. This product type is typically used as part of a skin care routine for people with acne-prone skin.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per g | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 8, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 49527-0045-01 You're viewing this Main listing | 1 TUBE in 1 CARTON / 125 mL in 1 TUBE | 2014-10-01 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 1P9D0Z171K
BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
-
UNII 3XUS85K0RA
Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
-
UNII 3G6A5W338E
Caffeine is a natural stimulant compound commonly extracted from coffee beans and tea leaves. In medicines, it serves as an active booster in pain relievers and cold products to enhance alertness and improve the effectiveness of other ingredients.
-
UNII 8NLQ36F6MM
Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
-
UNII MP1J8420LU
A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
-
UNII 9G34HU7RV0
EDTA is a chemical compound that binds to metals and other substances in medicines. It's used as a preservative and stabilizer to prevent discoloration and extend shelf life.
-
UNII H3R47K3TBD
FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
-
UNII S72O3284MS
A plant extract from the gentian root used as a flavoring agent and bitter taste component in some medicines. It helps mask unpleasant tastes and may support digestive formulations.
-
UNII PDC6A3C0OX
Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
-
UNII YSE9PPT4TH
Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
-
UNII 23D6XVI233
Lauramidopropyl betaine is a mild cleanser and foaming agent derived from coconut oil. In medicines, it helps create a smooth texture, reduce foam, and improve how the product spreads or mixes.
-
UNII V956696549
N-Acetylglucosamine is a naturally occurring sugar compound derived from chitin. In medicines, it typically serves as a filler or binding agent to help hold tablet ingredients together and add bulk to the formulation.
-
UNII YM0K64F20V
A synthetic emulsifier derived from polyethylene glycol and glucose. It helps blend oil and water-based ingredients together and improves the texture and spreadability of the product.
-
UNII HIE492ZZ3T
Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
-
UNII 68CMP2MB55
A brown seaweed extract used as a thickener and stabilizer in liquid medicines and suspensions. It helps maintain consistent texture and prevents ingredients from separating.
-
UNII 451W47IQ8X
Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
-
UNII 55X04QC32I
A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
-
UNII BPV390UAP0
Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
-
UNII C151H8M554
A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
-
UNII 1W6L629B4K
Sulisobenzone is a chemical UV filter used in some topical products to help protect against sun damage. It works as a sunscreen ingredient that absorbs ultraviolet light before it reaches the skin.
-
UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
21 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 6, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from CLINIQUE LABORATORIES LLC labeler code 49527
- REDNESS solutions DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15 TITANIUM DIOXIDE and ZINC OXIDE 65 mg/mL; 25 mg/mL Cream NDC 49527-019-01
- REPAIRWEAR UPLIFTING FIRMING BROAD SPECTUM SPF 15 - NORMAL COMBO TO COMBINATION oily OCTINOXATE, OCTISALATE, and TITANIUM DIOXIDE 75 mg/mL; 35 mg/mL; 17 mg/mL Cream NDC 49527-022-01
- CITY BLOCK SHEER Oil FREE DAILY FACE PROTECTOR BROAD SPECTRUM SPF 25 TITANIUM DIOXIDE and ZINC OXIDE 73 mg/mL; 69 mg/mL Cream NDC 49527-023-01
- EVEN BETTER MAKEUP BROAD SPECTRUM SPF 15 OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE 59 mg/mL; 35 mg/mL; 28 mg/mL Liquid NDC 49527-025-01
- MOISTURE SURGE CC BROAD SPECTRUM SPF 30 HYDRATING COLOUR CORRECTOR OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE 75 mg/mL; 50 mg/mL; 52 mg/mL; 32 mg/mL Cream NDC 49527-029-01
- Clinique Targeted Protection Spf 45 Broad Spectrum Sunscreen Homosalate, Octisalate, and Avobenzone 5 g/100g; 5 g/100g; 3 g/100g Stick NDC 49527-041-01
- CLINIQUE SMART CUSTOM REPAIR MOISTURIZER BROAD SPECTRUM SPF 15 - VERY DRY/DRY AVOBENZONE and OCTISALATE 30 mg/mL; 50 mg/mL Cream NDC 49527-048-01
- REPAIRWEAR LASER FOCUS LINE SMOOTHING BROAD SPECTRUM SPF 15 -VERY DRY TO DRY COMBINATION OCTINOXATE, OCTISALATE, and TITANIUM DIOXIDE .076125 g/100mL; .03745 g/100mL; .015225 g/100mL Cream NDC 49527-049-01
- CLINIQUE SMART CUSTOM REPAIR MOISTURIZER BROAD SPECTRUM SPF 15 - COMBINATION/OILY TO OILY AVOBENZONE and OCTISALATE 30 mg/mL; 50 mg/mL Cream NDC 49527-050-01
- CLINIQUE SMART BROAD SPECTRUM SPF 15 CUSTOM-REPAIR MOISTURIZER DRY COMBINATION avobenzone and octisalate 30 mg/mL; 50 mg/mL Cream NDC 49527-051-01
- ACNE AND LINE CORRECTING SERUM SALICYLIC ACID 10 mg/mL Lotion NDC 49527-053-01
- EVEN BETTER GLOW LIGHT REFLECTING MAKEUP BROAD SPECTRUM SPF 15 Octinoxate, Titanium Dioxide, and Zinc Oxide 60 mg/mL; 38 mg/mL; 30 mg/mL Lotion NDC 49527-056-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses treats acne clears acne blemishes helps prevent development of new acne blemishes
⏱️ Dosage and Administration ▾
Directions Wet hands and work into a lather Add water to increase lather Massage gently over wet skin, avoiding eye area Rinse Use A.M. and P.M. If bothersome drying or peeling occurs, reduce usage to every other day Follow with Acne Solutions Clarifying Lotion
⚠️ Warnings ▾
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 product is swallowed, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information Protect the product in this container from excessive heat and direct sun
🧪 Active Ingredient ▾
Active Ingredient Salicylic Acid 2%
🧪 Inactive Ingredients ▾
Inactive ingredients water\aqua\eau [] glycerin [] sodium laureth sulfate [] sodium chloride [] lauramidopropyl betaine [] butylene glycol [] sucrose [] gentiana lutea (gentian) root extract [] laminaria saccharina extract [] caffeine [] sodium hyaluronate [] acetyl glucosamine [] peg-120 methyl glucose dioleate [] benzophenone-4 [] sodium hydroxide [] tetrasodium edta [] disodium edta [] bht [] phenoxyethanol [] blue 1 (ci 42090) <iln50388>
🎯 Purpose ▾
Purpose Acne Treatment
📄 When Using This Product ▾
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 ▾
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 125 mL Tube Carton CLINIQUE acne solutions cleansing gel SALICYLIC ACID ACNE MEDICATION ALL SKIN TYPES
4.2FL.OZ.LIQ./125 ml e Principal Display Panel
Medicare Part D spend CMS · PART D · 2026 (Q1)
Reported adverse events (FAERS)
Top reported reactions
Age at onset
Reporter sex
Serious outcomes
Where does this data come from?
About this NDC listing & data coverage
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |