OTC Medication Information: Cloverine

CLOVERINE- petrolatum salve
Medtech Products Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Cloverine ® Brand Salve

Drug Facts

Active Ingredient

White Petrolatum 97%

Purpose

Skin protectant

Uses

Helps prevent and temporarily protects

  • chapped hands, face, lips
  • minor burns
  • windburn
  • chafing

Warnings

For external use only.

When using this product 

avoid contact with eyes.

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding

Ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • apply as needed

Inactive ingredients

fragrance, rectified turpentine oil, white wax

Other information

  • do not leave exposed to heat or direct sunlight.

Questions?

1-800-443-4908

PRINCIPAL DISPLAY PANEL

White
Cloverine
Brand

White petrolatum

Salve

1 oz. (28.4 g)

PRINCIPAL DISPLAY PANEL
White 
Cloverine
Brand
White petrolatum
Salve
1 oz. (28.4 g)
(click image for full-size original)
CLOVERINE
petrolatum salve
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63029-701
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PETROLATUM (PETROLATUM) PETROLATUM 27.6 g in 28.4 g
Inactive Ingredients
Ingredient Name Strength
TURPENTINE OIL
YELLOW WAX
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63029-701-01 1 CAN in 1 CARTON contains a CAN
1 28.4 g in 1 CAN This package is contained within the CARTON (63029-701-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part347 10/19/2010 08/31/2021
Labeler — Medtech Products Inc. (122715688)

Revised: 06/2020 Medtech Products Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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