enfuselle Acne Clarifying SALICYLIC ACID 5 mg/mL Lotion — NDC 59899-002-01 (Billing 59899-0002-01)
This is a package of enfuselle Acne Clarifying SALICYLIC ACID 5 mg/mL Lotion from Shaklee Corporation, marketed since Aug 2013 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 59899-002-01 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 59899 labeler · 002 product · 01 package
- Package marketed since
- Aug 8, 2013
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 5989900201 6
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 199134
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
RxNorm drug class
This medicine belongs to the Salicylic acid and derivatives class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 8, 2026
Clinical
Enfuselle Acne Clarifying is a topical lotion containing salicylic acid, an over-the-counter monograph drug marketed for acne care. Salicylic acid is commonly used in skin-care products to help exfoliate and clear pores. This lotion is applied directly to the skin as part of a routine skincare regimen for those dealing with acne-prone skin.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 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 9, 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 |
|---|---|---|---|---|
| 59899-0002-01 You're viewing this Main listing | 1 TUBE in 1 CARTON / 29 mL in 1 TUBE | 2013-08-08 | — | 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 9E8X80D2L0
A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
-
UNII L65MV77ZG6
A naturally occurring alcohol compound derived from plants, used as a fragrance and flavoring agent in medicines to improve taste and smell.
-
UNII ZY81Z83H0X
Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
-
UNII 597E9BI3Z3
Arctium lappa root is a plant-derived ingredient used in some traditional and herbal preparations. In formulations, it may serve as a natural extract or botanical agent to support product stability or flavor.
-
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 9M64UO4C25
A synthetic oily substance used as an emollient and texture enhancer in medicines. It helps soften formulations, improves how the medicine spreads or feels on skin, and can act as a lubricant in tablets or capsules.
-
UNII 7FLD91C86K
Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
-
UNII SL4SX1O487
A plant-derived polysaccharide used as a binder and thickener in medicines. It helps hold tablet ingredients together and can increase the viscosity of liquid formulations.
-
UNII CA2Y0FE3FX
A salt derived from licorice root extract, used as a flavoring agent and sweetener. It may also help soothe and protect mucous membranes in throat lozenges and cough products.
-
UNII M6QU9ZUH2X
A natural essential oil derived from the Manuka tree, used in medicines as a fragrance, flavor enhancer, and preservative to improve product appeal and shelf stability.
-
UNII YH89GMV676
A plant extract from watercress used as a natural flavoring or coloring agent in medications. It may help mask taste or add color to the formulation.
-
UNII WV9CM0O67Z
Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
-
UNII 68Y4CF58BV
Pyridoxine hydrochloride is a form of vitamin B6, added to medicines as a nutritional supplement or to meet dietary requirements. It supports the body's metabolism and nerve function.
-
UNII 9O3K93S3TK
Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
-
UNII 1D1K0N0VVC
A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
-
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.
-
UNII TTV12P4NEE
Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
-
UNII U6WSN5SQ1Z
Zinc gluconate is a form of zinc, a mineral, combined with gluconic acid. It's used as a supplement ingredient to provide zinc content in the formulation.
18 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 8, 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 Shaklee Corporation labeler code 59899
- enfuselle BODY SUNSCREEN BROAD SPECTRUM SPF 30 HOMOSALATE, OCTISALATE, AVOBENZONE, and OCTOCRYLENE 50 mg/mL; 30 mg/mL; 100 mg/mL; 100 mg/mL Lotion NDC 59899-007-01
- Youth 1 Activating BB Cream SPF 30 Light ZINC OXIDE, TITANIUM DIOXIDE 63 mg/mL; 23.6 mg/mL Lotion NDC 59899-010-01
- Youth 2 Activating BB Cream SPF 30 Light Medium ZINC OXIDE, TITANIUM DIOXIDE 63 mg/mL; 23.6 mg/mL Lotion NDC 59899-011-01
- Youth 3 Activating BB Cream SPF 30 Medium ZINC OXIDE, TITANIUM DIOXIDE 63 mg/mL; 23.6 mg/mL Lotion NDC 59899-012-01
- Youth 4 Activating BB Cream SPF 30 Dark ZINC OXIDE, TITANIUM DIOXIDE 63 mg/mL; 23.6 mg/mL Lotion NDC 59899-013-01
- Joint and Muscle Pain MENTHOL 50 mg/g Cream NDC 59899-022-00
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 For the treatment of acne.
⏱️ Dosage and Administration ▾
Directions for Use Clean the 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 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.
⚠️ Warnings ▾
Warnings For external use only.
🧪 Active Ingredient ▾
Active Ingredient Salicylic Acid (0.5%)
🧪 Inactive Ingredients ▾
INACTIVE INGREDIENTS Water/Eau, SD Alcohol 40-B, Cyclodextrin, Polysorbate 20, Xanthan Gum, 4-Terpineol*, Triethanolamine, Galactoarabinan, Zinc Gluconate, Sodium Coco PG-Dimonium Chloride Phosphate, Leptospermum Scoparium Branch/Leaf Oil, Tocopheryl Acetate, Dipostassium Glycyrrhizate, Panthenol, Disodium EDTA, Cetearyl Ethylhexanoate, Butylene Glycol, Nasturtium Officinale Extract, Arctium Lappa Root Extract, Aloe Barbadensis Leaf Juice, Pyridoxine HCL, Retinyl Palmitate.
🎯 Purpose ▾
Purpose Acne treatment
📄 When Using This Product ▾
When using this product Skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. If irritation occurs, use only one topical acne medication at a time. Keep out of eyes. Rinse with water to remove.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. In swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
Principal Labeling PARABEN FREE salicylic acid acne treatment 1fl. oz. 29mL 120applications All Skin Types This exclusive treatment formula gently and comprehensively controls the factors that contribute to the cycle of acne-troubled skin. Features an exclusive blend of nourishing antioxidants and purifying botanicals to help normalize sebum, unclog pores, speed healing, and reduce redness caused by acne.
With continued use, skin will become visibly smoother, clearer, and shine free. Shaklee Dist. by/par Shaklee Corporation 4747 Willow Road Pleasanton, CA 94588 USA Item #39075 • Breakthrough patented formula • Contains botanical extracts: - tea tree (Melaleuca alternifolia) oil - manuka (Leptospermum scoparium) oil - licorice (Dipotassium glycyrrhizate) extract - burdock (Arctium lappa) root extract - watercress (Nasturtium officinale) extract - aloe vera (Aloe barbadensis) leaf juice • Features antioxidant vitamins A and E • Gentle enough to use daily for maximum acne control • 100% fragrance and paraben free • Allergy tested • Clinically formulated • Dermatologist tested Do not store at temperatures above 10O°F.
U.S. Palent: 6,403,110 Apply this exclusive facial formula to help keep skin blemish free, speed healing and reduce redness caused by acne. Gentle enough to use daily, this unique blend of botanicals and nourishing antioxidants effectively controls the factors that contribute to the cycle of acnetroubled skin.
WARNINGS: For external use only. Keep out of eyes. “Keep out of reach of children. If excessive dryness or peeling occurs, reduce the application to once a day or every other day.
Directions: Apply one to three times daily after cleansing and toning. Allow to dry after application. Follow with the Enfuselle treatment or moisturizer for your skin type.
Not tested on animals 100% free of occlusive oils
Package Labeling: 1
Medicare Part D spend CMS · PART D · 2026 (Q1)
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. |