Label: BLOCKAID- lidocaine, tetracaine cream
- NDC Code(s): 82718-1110-1
- Packager: SofTap Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 6, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS
- PURPOSE
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OTHER INGREDIENTS
Deionized water, caprylc/capric triglyceride,stearic acid, glycerin, glyceryl stearate, petrolatum, safflower oil, shea butter, polysorbate 60, stearyl alcohol, sweet almond oil, tocopheryl acetate, bht, propylene glycol, sodium carbonate, phenoxyethanol, methylparaben, polyparaben. May contain: FD&C Green #3, FD&C Yellow #5, FD&C Blue #1
- USES
- DO NOT USE
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KEEP OUT OF
The eye and mouth. If accidental contact occurs, you may feel burning or stinging. Wash with water or eyewash immediately. If your eyes have pain, blurry vision, extreme sensitivity to light, or a feeling of sand in the eye, contact an eye care physician immediately.
WHEN USING THIS PRODUCT
You may not feel pain. Avoid sources of heat or injury.
You may have temporary rash, redness, swelling, or itching
Contact your physician promptly if you notice any unusual effects such as dizziness or drowsiness, difficulty breathing, trembling, chest pain, or irregular heartbeat.Made in the USA for SofTap
550 N Canyons Pkwy
Livermore, CA 94551
www.softaps.com
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DIRECTIONS
For external use only. Prior to application, a sensitivity test is advised. Before applying, cleanse the skin with an alcohol-free or acetone-free cleanser. Apply 1-2 cc to the desired area for up to 6 times per day. Discontinue use if allergic reaction occurs. Store in a cool dark place (up to 80 degrees F) or refrigerate.
- WARNINGS
- WARNINGS
- BLOCKAID
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INGREDIENTS AND APPEARANCE
BLOCKAID
lidocaine, tetracaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82718-1110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV) TETRACAINE 0.02 g in 10 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 0.03 g in 10 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) METHYLPARABEN (UNII: A2I8C7HI9T) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) SODIUM CARBONATE (UNII: 45P3261C7T) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) PETROLATUM (UNII: 4T6H12BN9U) STEARIC ACID (UNII: 4ELV7Z65AP) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALMOND OIL (UNII: 66YXD4DKO9) PROPYLPARABEN (UNII: Z8IX2SC1OH) SAFFLOWER OIL (UNII: 65UEH262IS) SHEA BUTTER (UNII: K49155WL9Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color blue (light blue) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82718-1110-1 10 g in 1 TUBE; Type 0: Not a Combination Product 05/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/06/2022 Labeler - SofTap Inc (780568353)
