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BRYTLY vs BANANA BABY: FdaNdcDirectoryPulse comparison
BRYTLY (2026-10-16) and BANANA BABY (2026-10-01) are peer FdaNdcDirectoryPulse records.
Data as of · Compiled by Zalwin from U.S. FDA National Drug Code (NDC) Directory via openFDA
Both records plus every comparable record, with all columns and source links · Card, Apple Pay, Google Pay or Link via Stripe
How does BRYTLY compare to BANANA BABY?
| Field | BRYTLY | BANANA BABY |
|---|---|---|
| Product | BRYTLY | BANANA BABY |
| Generic name | Apraclonidine Hydrochloride | AVOBENZONE,OCTISALATE,OCTOCRYLENE |
| NDC | 0065-8596 | 63354-852 |
| Labeler | Alcon Laboratories, Inc. | Edgewell Personal Care Brands LLC |
| Product type | HUMAN OTC DRUG | HUMAN OTC DRUG |
| Approval pathway | NDA | OTC MONOGRAPH DRUG |
| Application number | NDA220341 | M020 |
| Dosage form | SOLUTION/ DROPS | LOTION |
| Route | OPHTHALMIC | TOPICAL |
| Active ingredients | APRACLONIDINE HYDROCHLORIDE 1.25 mg/mL | OCTOCRYLENE 5.2 g/100g; AVOBENZONE 2.7 g/100g; OCTISALATE 4.5 g/100g |
| Marketing start | 2026-10-16 | 2026-10-01 |
| Package configurations | 3 | 1 |
| Launch Signal Score | 45/100 | 15/100 |
| Peer rank and all 500 records (CSV) | 🔒 Click to unlock → | |
| Official source URLs for every peer record | 🔒 Click to unlock → | |
Official records: BRYTLY · BANANA BABY
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Listing data comes from the FDA NDC directory via openFDA; a listing is not an FDA approval or endorsement and may be updated or withdrawn. Informational only; not medical advice.