Table 54: Pediculicides and Scabicides
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Drug Category: Dermatological
Medication Class/Individual Agents: Pediculicide/Scabicide
I. Prior-Authorization Requirements
Pediculicides and Scabicides |
Clinical Notes |
||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Please note: In the case where the prior authorization (PA) status column indicates PA, both the brand and generic (if available) require PA. Typically, the generic is preferred when available unless the brand-name drug appears on the MassHealth Brand Name Preferred Over Generic Drug List. In general, when requesting the non-preferred version, whether the brand or generic, the prescriber must provide medical records documenting an inadequate response or adverse reaction to the preferred version, in addition to satisfying the criteria for the drug itself.
Centers for Disease Control and Prevention: Treatment of Head Lice (2016)1
Centers for Disease Control and Prevention: Treatment of Scabies (2016)2
1.Centers for Disease Control and Prevention. Treatment of Head Lice [guideline on the internet]. 2016. [cited 2017 Feb 10]. Available at: https://www.cdc.gov/parasites/lice/head/treatment.html 2. Centers for Disease Control and Prevention. Treatment of Head Scabies [guideline on the internet]. 2016. [cited 2017 Feb 10]. Available at: http://www.cdc.gov/parasites/scabies/health_professionals/meds.html. |
# | This designates a brand-name drug with FDA “A”-rated generic equivalents. PA is required for the brand, unless a particular form of that drug (for example, tablet, capsule, or liquid) does not have an FDA “A”-rated generic equivalent. |
* | The generic OTC and, if any, generic prescription versions of the drug are payable under MassHealth without PA. |
II. Therapeutic Uses
FDA-approved, for example:
- Head lice (ivermectin lotion OTC, malathion, spinosad)
- Scabies (crotamiton lotion, Eurax cream)
Note: The above lists may not include all FDA-approved and non-FDA-approved indications.
III. Evaluation Criteria for Approval
- All PA requests must include clinical diagnosis, drug name, dose, and frequency.
- Dispensing in a 90-day supply of medication may be mandated or allowable for agents in this therapeutic class (designated by M90 or A90, respectively, in the Drug Notes section above). Applicable quantity limits are described below as units per day, per month, per 28 days, or as clinically appropriate, and may be extrapolated for fills of longer day supply.
- A preferred drug may be designated for this therapeutic class. In general, MassHealth requires a trial of the preferred drug or clinical rationale for prescribing a non-preferred drug within a therapeutic class. Additional information about these agents, including PA requirements and preferred products, can be found within the MassHealth Drug List at www.mass.gov/druglist.
- For recertification requests, approval may require submission of additional documentation including, but not limited to, documentation of: some or all criteria for the original approval; response to therapy; clinical rationale for continuation of use; status of member’s condition; appropriate diagnosis; appropriate age; appropriate dose, frequency, and duration of use for requested medication; complete treatment plan; current laboratory values; and member’s current weight.
- Additional criteria may apply depending upon diagnosis and/or requested medication (see below). Other factors, including rebate and FDA-approval status, may change independently of scheduled MassHealth updates, which may result in additional restrictions.
crotamiton lotion and Eurax cream
- Documentation of all of the following is required:
- appropriate diagnosis; and
- inadequate response to permethrin 5% within the last 30 days; or
- adverse reaction or contraindication to permethrin 5%; and
- inadequate response to oral ivermectin within the last 30 days; or
- adverse reaction or contraindication to oral ivermectin.
ivermectin lotion OTC and spinosad
- Documentation of all of the following is required:
- appropriate diagnosis; and
- member is ≥ six months of age; and
- inadequate response or adverse reaction to a permethrin product or a piperonyl butoxide/pyrethrins product within the last 30 days; or
- adverse reaction at any time or contraindication to both permethrin and piperonyl butoxide/pyrethrins products.
malathion
- Documentation of all of the following is required:
- appropriate diagnosis; and
- member is ≥ two years of age; and
- inadequate response or adverse reaction to a permethrin product or a piperonyl butoxide/pyrethrins product within the last 30 days; or
- adverse reaction at any time or contraindication to both of the following: permethrin product, piperonyl butoxide/pyrethrins product.
SmartPA: Claims for malathion will usually process at the pharmacy without a PA request if the member is ≥ two years of age and has a history of a paid MassHealth pharmacy claim for a permethrin product or a piperonyl butoxide/pyrethrins product within the last 30 days.†
Original Effective Date: 07/2011
Last Revised Date: 01/2025
Clinical Criteria Main Page | Back to top | Previous | Next
Last updated 01/06/25